Phenyl-isoxazoles as factor XA Inhibitors

ABSTRACT

The present application describes oxygen and sulfur containing heteroaromatics and derivatives thereof of formula                    
     or pharmaceutically acceptable salt or prodrug forms thereof, wherein J is O or S and D may be C(═NH)NH 2 , which are useful as inhibitors of factor Xa.

This application claims the benefit of U.S. Provisional Application No. 60/033,843, filed Dec. 23, 1996 and benefit of U.S. Provisional Application No. 60/050,975, filed Jun. 20, 1997.

FIELD OF THE INVENTION

This invention relates generally to oxygen or sulfur containing 5-membered ring heteroaromatics which are inhibitors of trypsin-like serine protease enzymes, especially factor Xa, pharmaceutical compositions containing the same, and methods of using the same as anticoagulant agents for treatment and prevention of thromboembolic disorders.

BACKGROUND OF THE INVENTION

WO 95/13155 and PCT International Application US 96/07692 describe isoxazoline and isoxazole fibrinogen receptor antagonists of the formula:

wherein R¹ may be a basic group, U—V may be a six-membered aromatic ring, W—X may be a variety of linear or cyclic groups, and Y is an oxy group. Thus, these compounds all contain an acid functionality (i.e., W—X—C(═O)—Y). In contrast, the presently claimed compounds do not contain such an acid functionality.

EP 0,513,387 depicts active oxygen inhibitors which are oxazoles or thiazoles of the formula:

wherein X is O or S, R² is preferably hydrogen, and both R¹ and R³ are substituted cyclic groups, with at least one being phenyl. The presently claimed invention does not relate to these types of oxazoles or thiazoles.

WO 95/18111 addresses fibrinogen receptor antagonists, containing basic and acidic termini, of the formula:

wherein R¹ represents the basic termini, U is an alkylene or heteroatom linker, V may be a heterocycle, and the right hand portion of the molecule represents the acidic termini. The presently claimed compounds do not contain the acidic termini of WO 95/18111.

In U.S. Pat. No. 5,463,071, Himmelsbach et al depict cell aggregation inhibitors which are 5-membered heterocycles of the formula:

wherein the heterocycle may be aromatic and groups A—B—C— and F—E—D— are attached to the ring system. A—B—C— can be a wide variety of substituents including a basic group attached to an aromatic ring. The F—E—D— group, however, would appear to be an acidic functionality which differs from the present invention. Furthermore, use of these compounds as inhibitors of factor Xa is not discussed.

Baker et al, in U.S. Pat. No. 5,317,103, discuss 5-HT₁ agonists which are indole substituted five-membered heteroaromatic compounds of the formula:

wherein R¹ may be pyrrolidine or piperidine and A may be a basic group including amino and amidino. Baker et al, however, do not indicate that A can be a substituted ring system like that contained in the presently claimed heteroaromatics.

Tidwell et al, in J. Med. Chem. 1978, 21(7), 613-623, describe a series of diarylamidine derivatives including 3,5-bis(4-amidinophenyl)isoxazole. This series of compounds was tested against thrombin, trypsin, and pancreatic kallikrein. The presently claimed invention does not include these types of compounds.

Activated factor Xa, whose major practical role is the generation of thrombin by the limited proteolysis of prothrombin, holds a central position that links the intrinsic and extrinsic activation mechanisms in the final common pathway of blood coagulation. The generation of thrombin, the final serine protease in the pathway to generate a fibrin clot, from its precursor is amplified by formation of prothrombinase complex (factor Xa, factor V, Ca²⁺ and phospholipid). Since it is calculated that one molecule of factor Xa can generate 138 molecules of thrombin (Elodi, S., Varadi, K.: Optimization of conditions for the catalytic effect of the factor Ixa-factor VIII Complex: Probable role of the complex in the amplification of blood coagulation. Thromb. Res. 1979, 15, 617-629), inhibition of factor Xa may be more efficient than inactivation of thrombin in interrupting the blood coagulation system.

Therefore, efficacious and specific inhibitors of factor Xa are needed as potentially valuable therapeutic agents for the treatment of thromboembolic disorders. It is thus desirable to discover new factor Xa inhibitors.

SUMMARY OF THE INVENTION

Accordingly, one object of the present invention is to provide novel oxygen or sulfur containing aromatic heterocycles which are useful as factor Xa inhibitors or pharmaceutically acceptable salts or prodrugs thereof.

It is another object of the present invention to provide pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.

It is another object of the present invention to provide a method for treating thromboembolic disorders comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.

These and other objects, which will become apparent during the following detailed description, have been achieved by the inventors, discovery that compounds of formula (I):

or pharmaceutically acceptable salt or prodrug forms thereof, wherein A, B, D, E, G, J, M, R^(1a), R^(1b), s and Z are defined below, are effective factor Xa inhibitors.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[1] Thus, in a first embodiment, the present invention provides novel compounds of formula I:

or a stereoisomer or pharmaceutically acceptable salt thereof, wherein;

ring M contains, in addition to J, 0-2 N atoms;

J is O or S;

D is selected from CN, C(═NR⁸)NR⁷R⁹, NHC(═NR⁸)NR⁷R⁹, NR⁸CH(═NR⁷), C(O)NR⁷R⁸, and (CR⁸R⁹)_(t)NR⁷R⁸, provided that D is substituted meta or para to G on E;

E is selected from phenyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, and piperidinyl substituted with 1 R;

alternatively, D—E—G together represent pyridyl substituted with 1 R;

R is selected from H, halogen, (CH₂)_(t)OR³, C₁₋₄ alkyl, OCF₃, and CF₃;

G is absent or is selected from NHCH₂, OCH₂, and SCH₂;

Z is selected from a C₁₋₄ alkylene, (CH₂)_(r)O(CH₂)_(r), (CH₂)_(r)NR³(CH₂)_(r), (CH₂)_(r)C(O)(CH₂)_(r), (CH₂)_(r)C(O)O(CH₂)_(r), (CH₂)_(r)OC(O)(CH₂)_(r), (CH₂)_(r)C(O)NR³(CH₂)_(r), (CH₂)_(r)NR³C(O)(CH₂)_(r), (CH₂)_(r)OC(O)O(CH₂)_(r), (CH₂)_(r)OC(O)NR³(CH₂)_(r), (CH₂)_(r)NR³C(O)O(CH₂)_(r), (CH₂)_(r)NR³C(O)NR³(CH₂)_(r), (CH₂)_(r)S(O)p(CH₂)_(r), (CH₂)_(r)SO2NR³(CH₂)_(r), (CH₂)_(r)NR³SO2(CH₂)_(r), and (CH₂)_(r)NR³SO2NR³(CH₂)_(r), provided that Z does not form a N—N, N—O, N—S, NCH₂N, NCH₂O, or NCH₂S bond with ring M or group A;

R^(1a) and R^(1b) are independently absent or selected from —(CH₂)_(r)—R¹′, NCH₂R¹″, OCH₂R¹″, SCH₂R¹″, N(CH₂)₂(CH₂)_(t)R¹′, O(CH₂)₂(CH₂)_(t)R¹′, and S(CH₂)₂(CH₂)_(t)R¹′, or combined to form a 5-8 membered saturated, partially saturated or unsaturated ring substituted with 0-2 R⁴ and which contains from 0-2 heteroatoms selected from the group consisting of N, O, and S;

R¹′ is selected from H, C₁₋₃ alkyl, halo, (CF₂)_(r)CF₃, OR², NR²R^(2a), C(O)R^(2c), OC(O)R², (CF₂)_(r)CO₂R^(2c), S(O)_(p)R^(2b), NR²(CH₂)_(r)OR², NR²C(O)R^(2b), NR²C(O)NHR^(2b), NR²C(O)₂R^(2a), OC(O)NR^(2b), C(O)NR²R^(2a), SO₂NR²R^(2a), NR²SO₂R^(2b), C₃₋₆ carbocyclic residue substituted with 0-2 R⁴, and 5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R⁴;

R¹′ is selected from H, C(O)R^(2b), C(O)NR²R^(2a), S(O)R^(2b), S(O)₂R^(2b), and SO₂NR²R^(2a);

R², at each occurrence, is selected from H, CF₃, C₁₋₆ alkyl, benzyl, C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b), and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R⁴b;

R^(2a), at each occurrence, is selected from H, CF₃, C₁₋₆ alkyl, benzyl, C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b), and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R^(4b);

R^(2b), at each occurrence, is selected from CF₃, C₁₋₄ alkoxy, C₁₋₆ alkyl, benzyl, C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b), and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R^(4b);

R^(2c), at each occurrence, is selected from CF₃, OH, C₁₋₄ alkoxy, C₁₋₆ alkyl, benzyl, C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b), and 5-6 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R^(4b);

alternatively, R² and R^(2a) combine to form a 5 or 6 membered saturated, partially saturated or unsaturated ring substituted with 0-2 R^(4b) which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R³, at each occurrence, is selected from H, C₁₋₄ alkyl, and phenyl;

R^(3a), at each occurrence, is selected from H, C₁₋₄ alkyl, and phenyl;

A is selected from:

C₃₋₁₀ carbocyclic residue substituted with 0-2 R⁴, and

5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R⁴;

B is selected from:

X—Y, NR²R^(2a), C(═NR²)NR²R^(2a), NR²C(═NR²)NR²R^(2a),

C₃₋₁₀ carbocyclic residue substituted with 0-2 R^(4a), and

5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R^(4a);

X is selected from C₁₋₄ alkylene, —CR²(CR²R^(2b))(CH₂)_(t)—, —C(O)—, —C(═NR)—, —CR²(NR¹″R²)—, —CR²(OR²)—, —CR²(SR²)—, —C(O)CR²R^(2a)—, —CR²R^(2a)C(O), —S(O)_(p)—, —S(O)_(p)CR²R^(2a)—, —CR²R^(2a)S(O)_(p)—, —S(O)₂NR²—, —NR²S(O)₂—, —NR²S(O)₂CR²R^(2a)—, —CR²R^(2a)S(O)₂NR²—, —NR²S(O)₂NR²—, —C(O)NR²—, —NR^(2a)(O)—, —C(O)NR²CR²R^(2a)—, —NR²C(O)CR²R^(2a)—, —CR²R^(2a)C(O)NR²—, —CR²R^(2a)NR²C(O)—, —NR²C(O)O—, —OC(O)NR²—, —NR²C(O)NR²—, —NR²—, —NR²CR²R^(2a)—, —CR²R^(2a)NR²—, O, —CR²R^(2a)O—, and —OCR²R^(2a)—;

Y is selected from:

(CH₂)_(r)NR²R^(2a), provided that X—Y do not form a N—N, O—N, or

S—N bond,

C₃₋₁₀ carbocyclic residue substituted with 0-2 R^(4a), and

5-10 membered heterocyclic system containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-2 R^(4a);

R⁴, at each occurrence, is selected from ═O, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, —CN, NO₂, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), NR²C(O)NR²R^(2a), CH(═NR²)NR²R^(2a), NHC(═NR²)NR²R^(2a), SO₂NR²R^(2a), NR²SO₂NR²R^(2a), NR²SO₂-C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, (CF₂)_(r)CF₃, NCH₂R¹″, OCH₂R¹″, SCH₂R¹″, N(CH₂)₂(CH₂)_(t)R¹′, O(CH₂)₂(CH₂)_(t)R¹′, and S(CH₂)₂(CH₂)_(t)R¹′,

alternatively, one R⁴ is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S;

R^(4a), at each occurrence, is selected from ═O, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, —CN, NO₂, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), NR²C(O)NR²R^(2a), CH(═NR²)NR²R^(2a), NHC(═NR²)NR²R^(2a), SO₂NR²R^(2a), NR²SO₂NR²R^(2a), NR²SO₂-O₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, and (CF₂)_(r)CF₃;

alternatively, one R^(4a) is a 5-6 membered aromatic heterocycle containing from 1-4 heteroatoms selected from the group consisting of N, O, and S substituted with 0-1 R⁵;

R^(4b), at each occurrence, is selected from ═O, (CH₂)_(r)OR³, halo, C₁₋₄ alkyl, —CN, NO₂, (CH₂)_(r)NR³R^(3a), (CH₂)_(r)C(O)R³, NR³C(O)R^(3a), C(O)NR³R^(3a), NR³C(O)NR³R^(3a), CH(═NR³)NR³R^(3a), NH³C(═NR³)NR³R^(3a), SO₂NR³R^(3a), NR³SO₂NR³R^(3a), NR³SO₂-C₁₋₄ alkyl, NR³SO₂CF₃, NR³SO₂-phenyl, S(O)_(p)CF₃, S(O)_(p)-C₁₋₄ alkyl, S(O)_(p)-phenyl, and (CF₂)_(r)CF₃;

R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl substituted with 0-2 R⁶, and benzyl substituted with 0-2 R⁶;

R⁶, at each occurrence, is selected from H, OH, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, CN, NO₂, (CH₂)_(r)NR²R^(2a),(CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), NR²C(O)NR²R^(2a), CH(═NH)NH₂, NHC(═NH)NH₂, SO₂NR²R^(2a), NR²SO₂NR²R^(2a), and NR²SO₂C₁₋₄ alkyl;

R⁷, at each occurrence, is selected from H, OH, C₁₋₆ alkyl, C₁₋₆ alkylcarbonyl, C₁₋₆ alkoxy, C₁₋₄ alkoxycarbonyl, (CH₂)_(n)-phenyl, C₆₋₁₀ aryloxy, C₆₋₁₀ aryloxycarbonyl, C₆₋₁₀ arylmethylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₆₋₁₀ arylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₁₋₆ alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C₁₋₄ alkoxycarbonyl;

R⁸, at each occurrence, is selected from H, C₁₋₆ alkyl and (CH₂)_(n)-phenyl;

alternatively, R⁷ and R⁸ combine to form a 5 or 6 membered saturated, ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R⁹, at each occurrence, is selected from H, C₁₋₆ alkyl and (CH₂)_(n)-phenyl;

n, at each occurrence, is selected from 0, 1, 2, and 3;

m, at each occurrence, is selected from 0, 1, and 2;

p, at each occurrence, is selected from 0, 1, and 2;

r, at each occurrence, is selected from 0, 1, 2, and 3;

s, at each occurrence, is selected from 0, 1, and 2; and,

t, at each occurrence, is selected from 0 and 1;

provided that D—E—G—(CH₂)_(s)— and —Z—A—B are not both benzamidines.

[2] In a preferred embodiment, the present invention provides novel compounds of formulae Ia-If:

wherein, groups D—E— and —Z—A—B are attached to adjacent atoms on the ring;

Z is selected from a CH₂O, OCH₂, CH₂NH, NHCH₂, C(O), CH₂C(O), C(O)CH₂, NHC(O), C(O)NH, CH₂S(O)₂, S(O)₂(CH₂), SO₂NH, and NHSO₂, provided that Z does not form a N—N, N—O, NCH₂N, or NCH₂O bond with ring M or group A;

A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R⁴;

phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, indazolyl, benzisoxazolyl, benzisothiazolyl, and isoindazolyl;

B is selected from: Y, X—Y, NR²R^(2a), C(═NR²)NR²R^(2a), and NR²C(═NR²)NR²R^(2a);

X is selected from C₁₋₄ alkylene, —C(O)—, —C(═NR)—, —CR²(NR²R^(2a))—, —C(O)CR²R^(2a)—, —CR²R^(2a)C(O), —C(O)NR²—, —NR²C(O)—, —C(O)NR²CR²R^(2a)—, —NR²C(O)CR²R^(2a)—, —CR²R^(2a)C(O)NR²—, —CR²R^(2a)NR²C(O)—, —NR²C(O)NR²—, —NR²—, —NR²CR²R^(2a)—, —CR²R^(2a)NR²—, O, —CR²R^(2a)O—, and —OCR²R^(2a)—;

Y is NR²R^(2a), provided that X—Y do not form a N—N or O—N bond;

alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a);

cylcopropyl, cyclopentyl, cyclohexyl, phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, benzofuranyl, benzothiofuranyl, indolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, indazolyl, benzisoxazolyl, benzisothiazolyl, and isoindazolyl;

alternatively, Y is selected from the following bicyclic heteroaryl ring systems:

 K is selected from O, S, NH, and N.

[3] In a more preferred embodiment, the present invention provides novel comopounds of formulae Ib and Ic:

wherein;

J is O or S; and,

Z is selected from a C(O), CH₂C(O), C(O)CH₂, NHC(O), C(O)NH, C(O)N(CH₃), CH₂S(O)₂, S(O)₂(CH₂), SO₂NH, and NHSO₂, provided that Z does not form a N—N or NCH₂N bond with ring M or group A.

[4] In an even more preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

E is phenyl substituted with R or 2-pyridyl substituted with R;

D is selected from NH₂, C(O)NH₂, C(═NH)NH₂, CH₂NH₂, CH₂NHCH₃, CH(CH₃)NH₂, and C(CH₃)₂NH₂, provided that D is substituted meta or para to ring M on E; and,

R is selected from H, OCH₃, Cl, and F.

[5] In a further preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

D—E is selected from 3-aminophenyl, 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-aminophenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-aminophenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl)phenyl, 6-aminopyrid-2-yl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, and 6-(2-amino-2-propyl)pyrid-2-yl.

[6] In another even more preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

Z is C(O)CH₂ and CONH, provided that Z does not form a N—N bond with group A;

A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2 R⁴; and,

B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R^(4a);

R⁴, at each occurrence, is selected from OH, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), and (CF₂)_(r)CF₃;

R^(4a) is selected from C₁₋₄ alkyl, CF₃, S(O)_(p)R⁵, SO₂NR²R^(2a), and 1-CF₃-tetrazol-2-yl;

R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl, and benzyl;

X is CH₂ or C(O) and,

Y is selected from pyrrolidino and morpholino.

[7] In another further preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,

B is selected from the group: 2-CF₃-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF₃-tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.

[8] In another even more preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

E is phenyl substituted with R or 2-pyridyl substituted with R;

D is selected from NH₂, C(O)NH₂, C(═NH)NH₂, CH₂NH₂, CH₂NHCH₃, CH(CH₃)NH₂, and C(CH₃)₂NH₂, provided that D is substituted meta or para to ring M on E; and,

R is selected from H, OCH₃, Cl, and F;

Z is C(O)CH₂ and CONH, provided that Z does not form a N—N bond with group A;

A is selected from phenyl, pyridyl, and pyrimidyl, and is substituted with 0-2 R⁴; and,

B is selected from X—Y, phenyl, pyrrolidino, morpholino, 1,2,3-triazolyl, and imidazolyl, and is substituted with 0-1 R^(4a);

R⁴, at each occurrence, is selected from OH, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), and (CF₂)_(r)CF₃;

R^(4a) is selected from C₁₋₄ alkyl, CF₃, S(O)_(p)R⁵, SO₂NR²R^(2a), and 1-CF₃-tetrazol-2-yl;

R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl, and benzyl;

X is CH₂ or C(O); and,

Y is selected from pyrrolidino and morpholino.

[9] In another further preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

D—E is selected from 3-aminophenyl, 3-amidinophenyl, 3-aminomethylphenyl, 3-aminocarbonylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-aminophenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-aminophenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, 4-fluoro-3-(methylaminomethyl)phenyl, 6-aminopyrid-2-yl, 6-amidinopyrid-2-yl, 6-aminomethylpyrid-2-yl, 6-aminocarbonylpyrid-2-yl, 6-(methylaminomethyl)pyrid-2-yl, 6-(1-aminoethyl)pyrid-2-yl, 6-(2-amino-2-propyl)pyrid-2-yl;

A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-pyrimidyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and,

B is selected from the group: 2-CF₃-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, 1-pyrrolidinocarbonyl, 2-(methylsulfonyl)phenyl, 4-morpholino, 2-(1′-CF₃-tetrazol-2-yl)phenyl, 4-morpholinocarbonyl, 2-methyl-1-imidazolyl, 5-methyl-1-imidazolyl, 2-methylsulfonyl-1-imidazolyl and, 5-methyl-1,2,3-triazolyl.

[10] In a still further preferred embodiment, the present invention provides a novel compound of formula Ib₁.

[11] In another still further preferred embodiment, the present invention provides a novel compound of formula Ib₂.

[12] In another still further preferred embodiment, the present invention provides a novel compound of formula Ib₃.

[13] In another still further preferred embodiment, the present invention provides a novel compound of formula Ib₄.

[14] In another still further preferred embodiment, the present invention provides a novel compound of formula Ic₁.

[15] In another still further preferred embodiment, the present invention provides a novel compound of formula Ic₂.

[16] In another even more preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

D is selected from C(═NR⁸)NR⁷R⁹, C(O)NR⁷R⁸, NR⁷R⁸, and CH₂NR⁷R⁸, provided that D is substituted meta or para to ring M on E;

E is phenyl substituted with R or pyridyl substituted with R;

R is selected from H, Cl, F, OR³, CH₃, CH₂CH₃, OCF₃, and CF₃;

Z is selected from C(O), CH₂C(O), C(O)CH₂, NHC(O), and C(O)NH, provided that Z does not form a N—N bond with ring M or group A;

R^(1a) and R^(1b) are independently absent or selected from —(CH₂)_(r)-R¹′, NCH₂R¹′, OCH₂R¹′, SCH₂R¹″, N(CH₂)₂(CH₂)_(t)R¹′, O(CH₂)₂(CH₂)_(t)R¹′, and S(CH₂)₂(CH₂)_(t)R¹′, or combined to form a 5-8 membered saturated, partially saturated or unsaturated ring substituted with 0-2 R⁴ and which contains from 0-2 heteroatoms selected from the group consisting of N, O, and S;

R¹′, at each occurrence, is selected from H, C₁₋₃ alkyl, halo, (CF₂)_(r)CF₃, OR², NR²R^(2a), C(O)R^(2c), (CF₂)_(r)CO₂R^(2c), S(O)_(p)R^(2b), NR²(CH₂)_(r)OR², NR²C(O)R^(2b), NR²C(O)₂R^(2b), C(O)NR²R^(2a), SO₂NR²R^(2a), and NR²SO₂R^(2b);

A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R⁴;

phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, and imidazolyl;

B is selected from: Y, X—Y, NR²R^(2a), C(═NR²)NR²R^(2a), and NR²C(═NR²)NR²R^(2a);

X is selected from CH₂, —CR²(CR²R^(2b))(CH₂)_(t)—, —C(O)—, —C(═NR)—, —CH(NR²R^(2a))—, —C(O)NR²—, —NR²C(O)—, —NR²C(O)NR²—, —NR²—, and O;

Y is NR²R^(2a), provided that X—Y do not form a N—N or O—N bond;

alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a);

phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, and 1,3,4-triazolyl;

R⁴, at each occurrence, is selected from ═O, OH, Cl, F, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), CH(═NH)NH₂, NHC(═NH)NH₂, SO₂NR²R^(2a), NR²SO₂-C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, and (CF₂)_(r)CF₃;

R^(4a), at each occurrence, is selected from ═O, OH, Cl, F, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), CH(═NH)NH₂, NHC(═NH)NH₂, SO₂NR²R^(2a), NR²SO₂-C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, (CF₂)_(r)CF₃, and 1-CF₃-tetrazol-2-yl;

R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl substituted with 0-2 R⁶, and benzyl substituted with 0-2 R⁶;

R⁶, at each occurrence, is selected from H, ═O, OH, OR², Cl, F, CH₃, CN, NO₂, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), CH(═NH)NH₂, NHC(═NH)NH₂, and SO₂NR²R^(2a);

R⁷, at each occurrence, is selected from H, OH, C₁₋₆ alkyl, C₁₋₆ alkylcarbonyl, C₁₋₆ alkoxy, C₁₋₄ alkoxycarbonyl, benzyl, C₆₋₁₀ aryloxy, C₆₋₁₀ aryloxycarbonyl, C₆₋₁₀ arylmethylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₆₋₁₀ arylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₁₋₆ alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C₁₋₄ alkoxycarbonyl;

R⁸, at each occurrence, is selected from H, C₁₋₆ alkyl and benzyl; and

alternatively, R⁷ and R⁸ combine to form a morpholino group; and,

R⁹, at each occurrence, is selected from H, C₁₋₆ alkyl and benzyl.

[17] In a another further preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

E is phenyl substituted with R or 2-pyridyl substituted with R;

R is selected from H, Cl, F, OCH₃, CH₃, OCF₃, and CF₃;

Z is selected from a C(O)CH₂ and C(O)NH, provided that Z does not form a N—N bond with group A;

R^(1a) is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2c), CH₂C(O)R^(2c), C(O)NR²R^(2a), and SO₂NR²R^(2a);

R^(1b) is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2c), CH₂C(O)R^(2c), C(O)NR²R^(2a), and SO₂NR²R^(2a);

A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R⁴;

phenyl, pyridyl, pyrimidyl, furanyl, thiophenyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, and imidazolyl;

B is selected from: Y and X—Y;

X is selected from CH₂, —CR²(CR²R^(2b))—, —C(O)—, —C(═NR)—, —CH(NR²R^(2a))—, —C(O)NR²—, —NR²C(O)—, —NR²C(O)NR²—, —NR²—, and O;

Y is NR²R^(2a), provided that X—Y do not form a N—N or O—N bond;

alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a);

phenyl, piperidinyl, piperazinyl, pyridyl, pyrimidyl, furanyl, morpholinyl, thiophenyl, pyrrolyl, pyrrolidinyl, oxazolyl, isoxazolyl, isoxazolinyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, thiadiazolyl, triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, and 1,3,4-triazolyl;

R², at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl;

R^(2a), at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl;

R^(2b), at each occurrence, is selected from CF₃, OCH₃, CH₃, benzyl, and phenyl;

R^(2c), at each occurrence, is selected from CF₃, OH, OCH₃, CH₃, benzyl, and phenyl;

alternatively, R² and R^(2a) combine to form a 5 or 6 membered saturated, partially unsaturated, or unsaturated ring which contains from 0-1 additional heteroatoms selected from the group consisting of N, O, and S;

R³, at each occurrence, is selected from H, CH₃, CH₂CH₃, and phenyl;

R^(3a), at each occurrence, is selected from H, CH₃, CH₂CH₃, and phenyl;

R⁴, at each occurrence, is selected from OH, Cl, F, CH₃, CH₂CH₃, NR²R^(2a), CH₂NR²R^(2a), C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), and CF₃;

R^(4a), at each occurrence, is selected from OH, Cl, F, CH₃, CH₂CH₃, NR²R^(2a), CH₂NR²R^(2a), C(O)R^(2b), C(O)NR²R^(2a), SO₂NR²R^(2a), S(O)_(p)R⁵, CF₃, and 1-CF₃-tetrazol-2-yl;

R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl substituted with 0-2 R⁶, and benzyl substituted with 1 R⁶;

R⁶, at each occurrence, is selected from H, OH, OCH₃, Cl, F, CH₃, CN, NO₂, NR²R^(2a), CH₂NR²R^(2a), and SO₂NR²R^(2a);

R⁷, at each occurrence, is selected from H, OH, C₁₋₃ alkyl, C₁₋₃ alkylcarbonyl, C₁₋₃ alkoxy, C₁₋₄ alkoxycarbonyl, benzyl, phenoxy, phenoxycarbonyl, benzylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, phenylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₁₋₆ alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C₁₋₄ alkoxycarbonyl;

R⁸, at each occurrence, is selected from H, CH₃, and benzyl; and,

alternatively, R⁷ and R⁸ combine to form a morpholino group;

R⁹, at each occurrence, is selected from H, CH₃, and benzyl.

[18] In a another still further preferred embodiment, the present invention provides novel compounds of formulae Ib and Ic, wherein;

R^(1a) is absent or is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), C(O)NR²R^(2a), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2c), CH₂C(O)R^(2c), and SO₂NR²R^(2a);

R^(1b) is absent or is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), C(O)NR²R^(2a), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2b), CH₂C(O)R^(2b), and SO₂NR²R^(2a);

A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R⁴;

phenyl, pyridyl, and pyrimidyl;

B is selected from: Y and X—Y;

X is selected from —C(O)— and O;

Y is NR²R^(2a), provided that X—Y do not form a O—N bond;

alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a);

phenyl, piperazinyl, pyridyl, pyrimidyl, morpholinyl, pyrrolidinyl, imidazolyl, and 1,2,3-triazolyl;

R², at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl;

R^(2a), at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl;

R^(2b), at each occurrence, is selected from CF₃, OCH₃, CH₃, benzyl, and phenyl;

R^(2c), at each occurrence, is selected from CF₃, OH, OCH₃, CH₃, benzyl, and phenyl;

alternatively, R² and R^(2a) combine to form a ring system selected from pyrrolidinyl, piperazinyl and morpholino;

R⁴, at each occurrence, is selected from Cl, F, CH₃, NR²R^(2a), and CF₃;

R^(4a), at each occurrence, is selected from Cl, F, CH₃, SO₂NR²R^(2a), S(O)_(p)R⁵, and CF₃; and,

R⁵, at each occurrence, is selected from CF₃ and CH₃.

[19] Specifically preferred compounds of the present invention invention is selected from the group:

3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1]-biphen-4-yl)aminocarbonyl]-5-(hydroxyrnethyl)isoxazole;

3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole;

3-(3-amidinophenyl)-4-[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole;

3-(3-amidinophenyl)-4-[5-(2-aminosulfonyl)phenylpyrid-2-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole;

3-(3-amidinophenyl)-4-[(2′-trifluoromethyl-[1,1]-biphen-4-yl)aminocarbonyl]isoxazole;

3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(trifluoromethyl)isoxazole;

2-acetylamino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-amino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-methyl-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

5-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]oxazole;

3-(3-amidinophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)amninocarbonyl]isoxazole;

3-(3-amidinophenyl)-4-[(2′-amninosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)-isoxazole;

3-(3-amidinophenyl)-4-[(2′-t-butylarinosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole;

3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole;

2-methyl-4-(3-amidinophenyl)-5-[(2′-trifluorornethyl-[1,1′]-biphen-4-yl)arninocarbonyl]thiazole;

2-phenyl-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

3-(3-amidinophenyl)-4-[(3-fluoro-2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole;

3-(3-amidinophenyl)-4-[(2′-trifluoromnethylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole;

3-(3-amidinophenyl)-5-amino-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole;

2-(phenylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-(benzylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-(methylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-(methylamino)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-methyl-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole;

2-methyl-4-(3-(carboxamido)phenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole;

2-(3-pyridyl)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-(3-pyridyl)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-chloro-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-chloro-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-chloro-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole;

2-chloro-4-(3-(carboxamido)phenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole;

2-hydroxy-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole;

2-chloro-4-(3-aminophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-amino-4-[(3-amino-4-chloro)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

2-chloro-4-[(3-amino-4-chloro)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole; and,

2-amino-4-[(3-aminomethyl)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole;

and a pharmaceutically acceptable salt thereof.

In a second embodiment, the present invention provides novel pharmaceutical compositions, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.

In a third embodiment, the present invention provides a novel method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.

DEFINITIONS

The compounds herein described may have asymmetric centers. Compounds of the present invention containing an asymmetrically substituted atom may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis from optically active starting materials. Many geometric isomers of olefins, C═N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. Cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomeric form is specifically indicated.

The term “substituted,” as used herein, means that any one or more hydrogens on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., ═O), then 2 hydrogens on the atom are replaced.

When any variable (e.g., R⁶) occurs more than one time in any constituent or formula for a compound, its definition at each occurrence is independent of its definition at every other occurrence. Thus, for example, if a group is shown to be substituted with 0-2 R⁶, then said group may optionally be substituted with up to two R⁶ groups and R⁶ at each occurrence is selected independently from the definition of R⁶. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

When a bond to a substituent is shown to cross a bond connecting two atoms in a ring, then such substituent may be bonded to any atom on the ring. When a substituent is listed without indicating the atom via which such substituent is bonded to the rest of the compound of a given formula, then such substituent may be bonded via any atom in such substituent. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

As used herein, “C₁₋₆ alkyl” is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, examples of which include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, pentyl, and hexyl; “Alkenyl” is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl, propenyl, and the like.

“Halo” or “halogen” as used herein refers to fluoro, chloro, bromo, and iodo; and “counterion” is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate, and the like.

As used herein, “carbocycle” or “carbocyclic residue” is intended to mean any stable 3- to 10-membered monocyclic or bicyclic or 7- to 13-membered bicyclic or tricyclic, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, cyclooctyl, [3.3.0]bicyclooctane, [4.3.0]bicyclononane, [4.4.0]bicyclodecane (decalin), [2.2.2]bicyclooctane, fluorenyl, phenyl, naphthyl, indanyl, adamantyl, or tetrahydronaphthyl (tetralin).

As used herein, the term “heterocycle” or “heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic ring which is saturated partially unsaturated or unsaturated (aromatic), and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O and S and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The nitrogen and sulfur heteroatoms may optionally be oxidized. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. If specifically noted, a nitrogen in the heterocycle may optionally be quaternized. It is preferred that when the total number of S and O atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another. It is preferred that the total number of S and O atoms in the heterocycle is not more than 1. As used herein, the term “aromatic heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic aromatic ring which consists of carbon atoms and from 1 to 4 heterotams independently selected from the group consisting of N, O and S. It is preferred that the total number of S and O atoms in the aromatic heterocycle is not more than 1.

Examples of heterocycles include, but are not limited to, 1H-indazole, 2-pyrrolidonyl, 2H,6H-1,5,2-dithiazinyl, 2H-pyrrolyl, 3H-indolyl, 4-piperidonyl, 4aH-carbazole, 4H-quinolizinyl, 6H-1,2,5-thiadiazinyl, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazalonyl, carbazolyl, 4aH-carbazolyl, β-carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl., oxazolyl, oxazolidinylperimidinyl, phenanthridinyl, phenanthrolinyl, phenarsazinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, piperidonyl, 4-piperidonyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, carbolinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, xanthenyl. Preferred heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, indolyl, benzimidazolyl, 1H-indazolyl, oxazolidinyl, benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl, or isatinoyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.

The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

As used herein, “pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.

The pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418, the disclosure of which is hereby incorporated by reference.

“Prodrugs” are intended to include any covalently bonded carriers which release the active parent drug according to formula (I) in vivo when such prodrug is administered to a mammalian subject. Prodrugs of a compound of formula (I) are prepared by modifying functional groups present in the compound in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compound. Prodrugs include compounds of formula (I) wherein a hydroxy, amino, or sulfhydryl group is bonded to any group that, when the prodrug or compound of formula (I) is administered to a mammalian subject, cleaves to form a free hydroxyl, free amino, or free sulfhydryl group, respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formula (I), and the like. Preferred prodrugs are amidine prodrugs wherein D is C(═NR⁷)NH₂, and R⁷ is selected from OH, C₁₋₄ alkoxy, C₆₋₁₀ aryloxy, C₁₋₄ alkoxycarbonyl, C₆₋₁₀ aryloxycarbonyl, C₆₋₁₀ arylmethylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, and C₆₋₁₀ arylcarbonyloxy C₁₋₄ alkoxycarbonyl. More preferred prodrugs are where R⁷ is OH, methoxy, ethoxy, benzyloxycarbonyl, methoxycarbonyl, and methylcarbonyloxymethoxycarbonyl.

“Stable compound” and “stable structure” are meant to indicate a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.

SYNTHESIS

The compounds of the present invention can be prepared in a number of ways known to one skilled in the art of organic synthesis. The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or by variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below. The reactions are performed in a solvent appropriate to the reagents and materials employed and suitable for the transformations being effected. It will be understood by those skilled in the art of organic synthesis that the functionality present on the molecule should be consistent with the transformations proposed. This will sometimes require a judgment to modify the order of the synthetic steps or to select one particular process scheme over another in order to obtain a desired compound of the invention. It will also be recognized that another major consideration in the planning of any synthetic route in this field is the judicious choice of the protecting group used for protection of the reactive functional groups present in the compounds described in this invention. An authoritative account describing the many alternatives to the trained practitioner is Greene and Wuts (Protective Groups In Organic Synthesis, Wiley and Sons, 1991). All references cited herein are hereby incorporated in their entirety herein by reference.

Schemes 1-4 describe the synthesis of compounds wherein M is furan and Q is a protected precursor of group D of formula I. Each scheme represents a different substitution pattern for the furan ring. In Scheme 1, an alpha-substituted carboxylic acid, wherein V is a nitro, protected sulfonamide or ester group, can be treated with two equivalents of base to activate it, quenched with an appropriate aldehyde electrophile as described by Wierenga (J. Org. Chem., 44(2), 310, 1979) and then oxidized by pyridinium dichromate to a ketone. Treatment with base and acetic anhydride should give the enol acetate which can react with a vinyl sulfoxide to give a dihydrofuran as shown by Chan (J. Chem. Soc., Perkins Trans. 1 1992, 945). This sulfoxide can then be oxidized and eliminated to give the desired furan.

In Scheme 2, the readily available bromides Q—E—Br are coupled to a terminal acetylene, to give a disubstituted alkyne as shown by Padwa (J. Org. Chem. 1991, 56(7), 2523). Also shown in Scheme 2, a carboxylic acid can be homologated into a ketone and then converted into a diazoketone. Rhodium catalyzed cyclization can provide the desired furan as in Davies (Tetrahedron 1988, 44(11), 3343).

Addition of a grignard reagent to the appropriate aldehyde, oxidation and O-methylation should give the required enol ether as shown in Scheme 3. Diazoketone formation of the acetyl derivative, AcW, and copper catalyzed cyclization can be done like Alonos (J. Org. Chem. 1991, 56(7), 2523) followed by standard deprotection should give the desired furan.

Scheme 4 describes a synthesis of a different substitution pattern on a furan ring. The carboxylic acid from above can be converted into a ketone in a two-step process by conversion to the activated acid chloride and reacting with a cuprate (Tetr. Lett. 1971, 829). Piperidine-catalyzed condensation with an appropriate aldehyde should give the unsaturated ketone as shown by Taylor (J. Het. Chem. 1989, 26, 1353). Conjugate addition of a dithiane to the unsaturated ketone should give the required substitution pattern. N-bromosuccinimide deprotection of the dithiane followed by acid-catalyzed cyclization can provide the furan.

Schemes 5 and 6 describe the synthesis of compounds wherein ring M is thiophene. The appropriate aldehyde in Scheme 5 can be oxidized to a carboxylic acid and converted to an acid chloride. Reaction of this acid chloride with methyl ketone and lithium bis(trimethylsilyl)amide as shown by Cushman (Tetr. Lett. 1990, 45, 6497). Further treatment with diazomethane can provide a mixture of two regioisomers which need not be separated at this time. Treatment of the commercially available bromide with sodium sulfide followed by the unsaturated ketone should give a mixture of thiophene regioisomers which can be separated according to Alberola (Synth. Comm. 1990, 20, 2537).

Alternatively, in Scheme 6, ethyl acetate can be diazotized by tosyl azide and carbene insertion into the E—Br bond as in D'yakonov (J. Gen. Chem. USSR, 1951, 21, 851). Nucleophilic displacement with a thiocarboxylic acid (Org. Syn. Coll. 1963, 4, 924) should give the appropriate carboxylic acid after basic hydrolysis as shown by Masuda (Chem. Pharm. Bull. 1977, 25, 1471). Reaction with a disubstituted alkyne with trifluoroacetic anhydride can give a mixture of regioisomers. By analogy switching the position of V and Q—E in the reagents can give a different set of regioisomers.

Schemes 7 and 8 provide routes to compounds of Formula I wherein ring M is isoxazole. Scheme 7 shows one possible synthesis of isoxazoles. Substituted benzaldehydes can be reacted with hydroxyl amine then chlorinated to give the hydroximinoyl chloride (see J. Org. Chem. 1980, 45, 3916). Preparation of the nitrile oxide in situ with triethylamine and cycloaddition with a substituted alkyne can give a mixture of regioisomeric isoxazoles as shown by H. Kawakami (Chem. Lett. 1987, 1, 85). Preparation of the disubstituted alkyne can be achieved by nucleophilic attack of the alkynyl anion on an electrophile as shown by L. N. Jungheim (J. Org. Chem. 1987, 57, 4007). Alternatively, one could make the hydroxyiminoyl chloride of the R^(1a) piece and react it with an appropriately substituted alkyne to give another set of regioisomeric isoxazoles which can be separated chromatographically.

An alternate procedure which should produce only one isoxazole regioisomer is described in Scheme 8. The methylated form of substituent V can be deprotonated and silylated. Chlorination with carbon tetrachloride or fluorination with difluorodibromomethane under triethylborane catalysis can give the geminal dihalo compound as shown by Sugimoto (Chem. Lett. 1991, 1319). Cuprate-mediated conjugate addition-elimination give the desired alkene as in Harding (J. Org. Chem. 1978, 43, 3874).

Alternatively, one can acylate with an acid chloride to form a ketone as in Andrews (Tetr. Lett. 1991, 7731) followed by diazomethane to form the enol ether. Each of these compounds can be reacted with a hydroximinoyl chloride in the presence of triethylamine to give one regioisomeric isoxazole as shown by Stevens (Tetr. Lett. 1984, 4587).

The following is a reaction grid for the synthesis of the Z linkage. The following coupling reaction would be readily known to those skilled in the art of organic synthesis.

When Z=

CONH then use V═CO₂CH₃ and W═NH₂ under AlMe₃ catalysis

SO₂NH then make heterocycle after sulfonamide formation

CH₂NH then reduce V═CO₂CH₃ with DIBAL to CH₂OH and couple with W═NH₂ using PPh₃

CH₂S then reduce V═CO₂CH₃ with DIBAL to CH₂OH and couple with W═SH using MsCl

CH₂O then reduce V═CO₂CH₃ with DIBAL to CH₂OH and couple with W═OH using PPh₃

NHCO then reduce V═NO₂ to NH₂ using H₂/Pd and couple with W═CO₂CH₃ using AlMe₃

NHSO₂ then reduce V═NO₂ to NH₂ using H₂/Pd and couple with W═SO₂Cl

NHCH₂ then reduce V═NO₂ to NH₂ using H₂/Pd and couple with W═CH₂Br

OCH₂ then reduce, then diazotize V═NO₂ and couple with W═CH₂Br

SCH₂ then reduce V═SO₂NR₂ with LAH and couple with W═CH₂Br.

To complete the final reaction sequence, substituent Q can be deprotected or reacted to give an amine or amide. The amine can converted into an amidine, guanidine or formamidine under standard conditions as outline in Scheme 9. From the nitrile, imididate formation followed by amination with ammonium carbonate can provide the amidine.

The compounds of Formula I in which ring M is thiazole or oxazole can be prepared as outlined in Schemes 10-16 wherein, R^(e) and R^(f) can be Z—A—B or R^(1a) or precursors thereof. There are numerous methods by which to prepare and manipulate substituted thiazole and oxazole rings (for reviews, see Comprehensive Heterocyclic Chemistry, Katritzky and Rees, eds. 1984, 6, 247 and Chem. Het. Cmpds. 1979, 34-2, 1). One particularly useful method for preparing thiazole and oxazole containing compounds of the present invention is the Hantzsch method, which involves condensation of α-haloketones with thioamides, thioureas, amides and ureas.

As shown in Scheme 10, an appropriate ketone can be brominated by a variety of electrophilic brominating reagents such as pyridinium bromide perbromide, NBS, etc. to afford an α-bromoketone. Heating with a wide variety of substituted thioamides and thioureas, and amides and ureas can afford thiazole and oxazole derivatives. Regioisomeric thiazoles and oxazoles can be prepared by a similar reaction sequence beginning with a similar ketone. The ketones in Scheme 10 are readily available by procedures familiar to those skilled in the art of organic synthesis. The functionality Q can later be transformed into the group D found in compounds of Formula I.

The thioamides are either commercially available or can be prepared from the corresponding amides using Lawesson's reagent or phosphorous pentasulfide. They can also be prepared and cyclized in situ by performing the cyclization reaction with the corresponding amide in the presence of phosphorous pentasulfide. The thioureas are either commercially available or are readily prepared from other commercially available thioureas. The amides and ureas are either commercially available or are readily prepared by procedures known to those skilled in the art.

In Scheme 11 is shown how α-acylaminoketones can be converted into oxazoles by dehydration with an acid such as sulfuric acid. Treating with phosphorous pentasulfide can afford thiazoles. The starting materials are prepared by standard methods known to those skilled in the art.

Oxazoles can also be prepared by the cyclization strategy shown in Scheme 12. Ketones can be converted into their oxime derivatives by standard treatment with hydroxylamine. Treating these intermediates with acid chlorides can provide the corresponding oxazoles.

2-Unsubstituted oxazoles can be prepared by the cyclization shown in Scheme 13. Treatment of acid chlorides with an isocyanoacetate (wherein R^(g) can be A—B or a precursor thereof) in the presence of a base such as triethylamine can afford the oxazoles (Suzuki et. al. Syn. Comm. 1972, 2, 237).

Other cyclization strategies can afford differently substituted thiazoles and oxazoles. In Scheme 14 is shown how cyclizations can be modified to afford 5-aminooxazoles and 4-and 5-aminothiazoles. Treatment of aldehydes with NaCN and ammonium chloride can afford α-aminonitriles (Steiger Org. Syn. Coll. Vol. III 1955, 84). Acylation with acid chlorides followed by acid-catalyzed dehydration can afford 5-aminooxazoles. The bromination of nitrites with bromine can afford α-bromonitriles. These can be treated with a variety of thioamides to afford 4-aminothiazoles. The 5-aminothiazoles can be prepared by elaboration of thiazole carboxylic acids. Formation of the acyl azide by standard methods can be followed by heating to effect a Curtius rearrangement to give the isocyanate (South, J. Het. Chem. 1991, 28, 1003). Addition of water can then afford the 5-aminothiazoles.

In Scheme 15 is shown how thiazoles and oxazoles with halogen substituents can be prepared. The 2-halo- derivatives can be prepared from the corresponding amino derivatives by diazotization with nitrous acid or isoamyl nitrite followed by displacement with an appropriate halide source such as copper bromide or chloride. The 5-halo- derivatives can be prepared by ring bromination with NBS or Br₂, or chlorination with NCS or Cl₂. Alternatively, the Hunsdiecker procedure (Ber. 1942, 75, 291) can be applied to the 5-carboxylic acid derivatives to prepare the bromides. The 4-halo derivatives can be prepared in the same manner from the regioisomer in which the group Q—E occupies position 5 on the ring.

In Scheme 16 is shown how mercapto and sulfonyl derivatives of the thiazoles and oxazoles can be prepared. The 2-mercapto derivatives can be prepared from the corresponding 2-amino heterocycles by diazotization with nitrous acid or isoamyl nitrite followed by reaction with an appropriate thiol. Oxidation of the thiol derivative can afford the sulfonic acid derivatives. The 5-mercapto derivatives can be prepared by thiol displacement of the appropriate 5-bromo derivative. Alternatively, halogen metal exchange of the bromo derivative with n-BuLi followed by quenching with sulfur can afford the required 5-mercapto derivatives. The sulfonyl derivatives are available by oxidation of the mercapto derivatives. In some cases direct sulfonation of the thiazole or oxazole ring can be possible. When R′ is an activating group such as amino or alkoxy, treatment with chlorosulfonic acid should give the sulfonyl derivative (Mann et. al. J. Prakt. Chem. 1978, 320, 715). The 4-mercapto and sulfonyl derivatives can be prepared in the same manner as shown for the 5-derivatives from the regioisomers in which the group Q—E occupies position 5 on the ring.

By the cyclization strategies described in Schemes 10-16, and by other strategies not described but familiar to those skilled in the art of organic synthesis, a wide variety of highly substituted thiazoles and oxazoles can be prepared. Proper manipulation of the starting materials for these cyclizations by procedures known to those skilled in the art also allows for the synthesis of oxazoles (Scheme 17, J=O) and thiazoles (Scheme 17, J=S), which are regioisomers of the thiazoles and oxazoles of Scheme 10, containing a wide variety of substituents R^(e) and R^(f) which by proper manipulation described in preceeding and following schemes can be converted into R^(1a) and Z—A—B of compounds of Formula I.

The present invention also describes compounds of Formula I in which ring M is 1,2,3- and 1,2,5-thiadiazole and 1,2,5-oxadiazole. The following schemes provide methods for synthesizing these heterocycles. In Scheme 18 is shown how 1,2,3-thiadiazoles can be prepared. The ketones from Scheme 10 can be converted by standard procedures into semicarbazones (R^(f)=NH₂) or acylhydrazones (R^(f)=alkyl, alkoxy) which can then be treated with thionyl chloride to prepare the 1,2,3-thiadiazoles (J. Med. Chem. 1985, 28, 442). Alternatively, diazo ketones can be prepared by treatment with base and a suitable diazo transfer reagent such as tosyl azide. Treatment of these diazo intermediates with hydrogen sulfide or Lawesson's reagent can afford the 1,2,3-thiadiazoles.

In Scheme 19 is shown how to prepare the 1,2,5-thiadiazoles contained in compounds of Formula I. The disubstituted alkynes, which are readily available by standard alkyne coupling procedures known to those skilled in the art of organic synthesis, can be treated with sulfur nitride in refluxing toluene to afford the 1,2,5-thiadiazoles(J. Het. Chem. 1979, 16, 1009).

In Scheme 20 is shown how 1,2,5-oxadiazole heterocycles can be prepared. Diazotization of ketones followed by treatment with hydroxylamine can afford the bisoximes. Alternatively, diketones can be treated with hydroxylamine to afford the bisoximes. Dehydration of these readily prepared intermediates with acetic acid or thionyl chloride can then afford the 1,2,5-oxadiazoles.

In the cyclization sequences and strategies described above, in general the substituents Q—E and R^(e) and R^(f) can be varied widely. In some cases R^(e) can be chosen so that it corresponds to Z—A—B in Formula I. In other cases R^(b) can be chosen so that it is hydrogen, carboxylic ester, amino, alkyl, cyano, alkoxy, hydroxy, thioalkoxy, sulfonyl, etc. which can subsequently be converted into the group Z—A—B of Formula I.

In the following schemes are described some methods by which the various groups Z of Formula I can be prepared from various groups R^(e). In these schemes the heterocycle is denoted as ring M and it is understood that the reactions described will generally be applicable to all of the different heterocycles previously described. It is also understood that the reactions described may require some modification of the reaction conditions, change in the reaction order or suitable protecting groups, depending upon the functionality contained in the compound of interest. One skilled in the art of organic synthesis will understand this and be able to modify the reaction sequence to obtain the desired products.

In Scheme 21 is shown how the heterocyclic compounds from above where R^(e) is a carboxylic ester group can be converted into compounds containing the Z—A—B residue. For the amide linker (Formula I, Z=—CONH—) ring M where R^(e) =carboalkoxy can be hydrolyzed to the acid. Formation of the acid chloride with thionyl chloride followed by the addition of an appropriate amine H₂N—A—B can afford the amide-linked compounds. Alternatively, the acid can be combined with the amine H₂N—A—B in the presence of a suitable peptide coupling agent, such as BOP-Cl, HBTU or DCC to afford the corresponding amides. In another method the ester can be directly coupled with an aluminum reagent, prepared by the addition of trimethylaluminum to the amine H₂N—A—B, to afford the amide. To form ether- and thioether-linked compounds of Formula I (Z=—CH₂O—, —CH₂S—) the acid can be reduced to the alcohol. Preferred procedures for this transformation are reduction with borane THF complex, or a procedure involving the reduction of the mixed anhydride of the acid with sodium borohydride. Completion of the ether and thioether linked compounds of Formula I can be readily accomplished by the Mitsonobu protocol with an appropriate phenol, thiophenol or hydroxy- or mercaptoheterocycle HZ—A—B (Formula I, A=aryl or heteroaryl). Other ethers or thioethers can be prepared following initial conversion of the alcohol to a suitable leaving group, such as tosylate. Where J═S, thioethers can be further oxidized to prepare the sulfones (Formula I, Z=—CH₂SO₂—). To prepare the amine-linked compounds of Formula I (Z=—CH₂NH—) the alcohol can be oxidized to the aldehyde by a number of procedures, two preferred methods of which are the Swern oxidation and oxidation with pyridinium chlorochromate (PCC). Reductive amination of aldehyde with an appropriate amine H₂N—A—B and sodium cyanoborohydride can then afford the amine linked compounds. The aldehyde also can be used to prepare the ketone-linked compounds of Formula I (Z=—COCH₂—). Treatment of the aldehyde with an organometallic species can afford the alcohol. The organo metallic species (where M=magnesium or zinc) can be best prepared from the corresponding halide by treatment with metallic magnesium or zinc. These reagents readily react with aldehydes to afford alcohols. Oxidation of the resulting alcohol by any of a number of procedures, such as the Swern oxidation or PCC oxidation, can afford the ketone.

Additional compounds of Formula I in which the linking group Z contains a nitrogen atom attached to ring M can be prepared by the procedures described in Scheme 22. The amines can be converted to the sulfonamides (Formula I, Z=—NHSO₂—) by treatment with an appropriate sulfonyl chloride B—A—SO₂Cl in the presence of a base such as triethylamine. The amines can be converted into the amides (Formula I, Z=—NHCO—) by treatment with an appropriate acid chloride Cl—CO—A—B in the presence of a base or by treatment with an appropriate carboxylic acid HO—CO—A—B in the presence of a suitable peptide coupling agent, such as DCC, HBTU or BOP-Cl. The amine can be converted into amines of Formula I (Z=—NHCH₂—) by reductive amination with an appropriate aldehyde OHC—A—B.

Additional compounds of Formula I in which the linking group Z contains a sulfur atom attached to ring M can be prepared by the procedures described in Scheme 23. Treatment of sulfonyls with phosphorous pentachloride followed by treatment with an appropriate amine H₂N—A—B can afford the sulfonamide-linked compounds (Formula I, Z=—SO₂NH—). The thiols can be alkylated with a suitable alkylating reagent in the presence of a base to afford thioethers (Formula I, Z=—SCH₂—). These compounds can be further oxidized by a variety of reagents to afford the sulfone-linked compounds (Formula I, Z=—SO₂CH₂—).

Compounds of this invention where B is either a carbocyclic or heterocyclic residue as defined in Formula I are coupled to A as shown generically and by specific example in Scheme 24, either or both of A and B may be substituted with 0-2 R⁴. W is defined as a suitable protected nitrogen, such as NO₂ or NHBOC; a protected sulfur, such as S-tBu or SMOM; or a methyl ester. Halogen-metal exchange of the bromine in bromo-B with n-butyl lithium, quenching with triisopropyl borate and acidic hydrolysis should give the required boronic acid, B′·B(OH)₂. The W—A—Br subunit may be already linked to ring M before the Susuki coupling reaction. Deprotection can provide the complete subunit.

Scheme 25 describes a typical example of how the A—B subunit can be prepared for attachment to ring M. 4-Bromoaniline can be protected as Boc-derivative and the coupled to 2-(t-butylamino)sulfonylphenylboronic acid under Suzuki conditions. 2-(t-Butylamino)sulfonylphenylboronic acid can be prepared by the method described by Rivero (Bioorg. Med. Chem. Lett. 1994, 189). Deprotection with TFA can provide the aminobiphenyl compound. The aminobiphenyl can then be coupled to the core ring structures as described below.

When B is defined as X—Y, the following description applies. Groups A and B are available either through commercial sources, known in the literature or readily synthesized by the adaptation of standard procedures known to practioners skilled in the art of organic synthesis. The required reactive functional groups appended to analogs of A and B are also available either through commercial sources, known in the literature or readily synthesized by the adaptation of standard procedures known to practioners skilled in the art of organic synthesis. In the tables that follow the chemistry required to effect the coupling of A to B is outlined.

TABLE A Preparation of Amide, Ester, Urea, Sulfonamide and Sulfamide linkages between A and B. then the reactive to give the Rxn. substituent of following product No. if A contains: Y is: A-X-Y: 1 A-NHR² as a ClC(O)-Y A-NR₂-C(O)-Y substituent 2 a secondary NH ClC(O)-Y A-C(O)-Y as part of a ring or chain 3 A-OH as a ClC(O)-Y A-O-C(O)-Y substituent 4 A-NHR² as a ClC(O)-CR²R^(2a)-Y A-NR²-C(O)CR²R^(2a)-Y substituent 5 a secondary NH ClC(O)-CR²R^(2a)-Y A-C(O)-CR²R^(2a)-Y as part of a ring or chain 6 A-OH as a ClC(O)-CR²R^(2a)-Y A-O-C(O)-CR²R^(2a)-Y substituent 7 A-NHR³ as a ClC(O)NR²-Y A-NR²-C(O)NR²-Y substituent 8 a secondary NH ClC(O)NR²-Y A-C(O)NR²-Y as part of a ring or chain 9 A-OH as a ClC(O)NR²-Y A-O-C(O)NR²-Y substituent 10 A-NHR² as a ClSO²-Y A-NR²-SO₂-Y substituent 11 a secondary NH ClSO₂-Y A-SO₂-Y as part of a ring or chain 12 A-NHR² as a ClSO₂-CR²R^(2a)-Y A-NR₂-SO₂-CR²R^(2a)-Y substituent 13 a secondary NH ClSO₂-CR²R^(2a)-Y A-SO₂-CR²R^(2a)-Y as part of a ring or chain 14 A-NHR² as a ClSO₂-NR²-Y A-NR²-SO₂-NR²-Y substituent 15 a secondary NH ClSO₂-NR²-Y A-SO₂-NR²-Y as part of a ring or chain 16 A-C(O)Cl HO-Y as a A-C(O)-O-Y substituent 17 A-C(O)Cl NHR₂-Y as a A-C(O)-NR²-Y substituent 18 A-C(O)Cl a secondary NH A-C(O)-Y as part of a ring or chain 19 A-CR²R^(2a)C(O)Cl HO-Y as a A-CR²R^(2a)C(O)-O-Y substituent 20 A-CR²R^(2a)C(O)Cl NHR²-Y as a A-CR²R^(2a)C(O)-NR²-Y substituent 21 A-CR²R^(2a)C(O)Cl a secondary NH A-CR²R^(2a)C(O)-Y as part of a ring or chain 22 A-SO₂Cl NHR²-Y as a A-SO₂-NR²-Y substituent 23 A-SO₂Cl a secondary NH A-SO₂-Y as part of a ring or chain 24 A-CR²R^(2a)SO₂Cl NHR²-Y as a A-CR²R^(2a)SO₂-NR²-Y substituent 25 A-CR²R^(2a)SO₂Cl a secondary NH A-CR²R^(2a)SO₂-Y as part of a ring or chain

The chemistry of Table A can be carried out in aprotic solvents such as a chlorocarbon, pyridine, benzene or toluene, at temperatures ranging from −20° C. to the reflux point of the solvent and with or without a trialkylamine base.

TABLE B Preparation of ketone linkages between A and B. then the reactive to give the Rxn. substituent of following product No. if A contains: Y is: A-X-Y: 1 A-C(O)Cl BrMg-Y A-C(O)-Y 2 A-CR²R^(2a)C(O)Cl BrMg-Y A-CR²R^(2a)2C(O)-Y 3 A-C(O)Cl BrMgCR²R^(2a)-Y A-C(O)CR²R^(2a)-Y 4 A-CR²R^(2a)C(O)Cl BrMgCR²R^(2a)-Y A-CR²R^(2a)C(O)CR²R^(2a)-Y

The coupling chemistry of Table B can be carried out by a variety of methods. The Grignard reagent required for Y is prepared from a halogen analog of Y in dry ether, dimethoxyethane or tetrahydrofuran at 0° C. to the reflux point of the solvent. This Grignard reagent can be reacted directly under very controlled conditions, that is low temeprature (−20° C. or lower) and with a large excess of acid chloride or with catalytic or stoichiometric copper bromide-dimethyl sufide complex in dimethyl sulfide as a solvent or with a variant thereof. Other methods available include transforming the Grignard reagent to the cadmium reagent and coupling according to the procedure of Carson and Prout (Org. Syn. Col. Vol. 3 (1955) 601) or a coupling mediated by Fe(acac)₃ according to Fiandanese et al (Tetrahedron Lett., (1984) 4805), or a coupling mediated by manganese (II) catalysis (Cahiez and Laboue, Tetrahedron Lett., 33(31), (1992) 4437).

TABLE C Preparation of ether and thioether linkages between A and B then the reactive to give the Rxn. substituent of following product No. if A contains: Y is: A-X-Y: 1 A-OH Br-Y A-O-Y 2 A-CR²R^(2a)-OH Br-Y A-CR²R^(2a)O-Y 3 A-OH Br-CR²R^(2a)-Y A-OCR²R^(2a)-Y 4 A-SH Br-Y A-S-Y 5 A-CR²R^(2a)-SH Br-Y A-CR²R^(2a)S-Y 6 A-SH Br-CR²R^(2a)-Y A-SCR²R^(2a)-Y

The ether and thioether linkages of Table C can be prepared by reacting the two components in a polar aprotic solvent such as acetone, dimethylformamide or dimethylsulfoxide in the presence of a base such as potassium carbonate, sodium hydride or potassium t-butoxide at temperature ranging from ambient temperature to the reflux point of the solvent used.

TABLE D Preparation of —SO— and —SO₂— linkages from thioethers of Table 3. and it is oxidized and it is oxidized with m-chloroper- with Alumina (wet)/ benzoic acid (Satoh if the Oxone (Greenhalgh, et al., Chem. Lett. Rxn. starting Synlett, (1992( 235) (1992) 381), the No. material is: the product is: product is: 1 A-S-Y A-S(O)-Y A-SO₂-Y 2 A-CR²R^(2a)S-Y A-CR²R^(2a)S(O)-Y A-CR²R^(2a)SO₂-Y 3 ASCR²R^(2a)-Y A-S(O)CR²R^(2a)-Y A-SO₂-CR²R^(2a)-Y

The thioethers of Table C serve as a convenient starting material for the preparation of the sulfoxide and sulfone analogs of Table D. A combination of wet alumina and oxone can provide a reliable reagent for the oxidation of the thioether to the sulfoxide while m-chloroperbenzoic acid oxidation will give the sulfone.

Other features of the invention will become apparent in the course of the following descriptions of exemplary embodiments which are given for illustration fo the invention and are not intended to be limiting thereof.

EXAMPLES Example 1 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(hydroxymethyl)isoxazole, trifluoroacetic acid salt

Part A. Preparation of 2-(t-butylaminosulfonyl)phenylboronic acid.

To a solution of 206.5 g (0.968 mol) of benzene-(N-t-butyl)sulfonamide in 2500 mL of THF under N₂ was added 790 mL (1.98 mol) of 2.5M n-butyllithium in hexane over 35 minutes, keeping the temperature between 0-5° C. The reaction mixture was allowed to warm to 10° C., at which time a thick precipitate formed. Triisopropylborate (305 mL, 1.32 mol) was added keeping the temperature below 35° C. After 1 hour, the reaction mixture was cooled, 1N HCl (1570 mL) was added, and the mixture was stirred overnight. The mixture was extracted with 400 mL of ether three times, and the combined organic extracts were extracted with 500 mL of 1N NaOH three times. The aqueous extracts were acidified to pH 1 with 6N HCl, and then extracted with 500 mL ether three times. The combined ether extracts were dried over MgSO₄, and the solvents evaporated in vacuo until the volume was 700 mL. Hexane (150 mL) was added and overnight, a white precipitate formed. The solid was collected and washed with 10% ether/hexane (250 mL), then dried in vacuo to give 216.3 g (87%) of the desired compound as white crystals. m.p. 118-119° C. ¹H NMR (CDCl₃) δ: 8.00 (d, 1H); 7.82 (d, 1H); 7.53 (m, 2H); 6.29 (br s, 2H); 5.13 (s, 1H); 1.18 (s, 9H).

Part B. Preparation of N-(4-bromophenyl)-4-(tetrahydropyran-2-yloxymethyl)-2-butynamide.

To a solution of 4.98 g (35.5 mmol) of tetrahydro-2-(2-propynyloxy)-2H-pyran in 70 mL of THF under N₂ was added 14.2 mL (35.5 imol) of 2.5 M n-butyllithium in hexane. After 15 minutes, 7.03 g (35.5 mmol) of 4-bromophenylisocyanate was added and then the reaction was allowed to warm to room temperature. Saturated aqueous ammonium chloride (20 mL) was added and the mixture extracted with 30 mL ethyl acetate three times. The combined organic extracts were dried with MgSO₄, concentrated to an oil in vacuo and then chromatographed on silica with 20% EtOAc/hexane to give 7.1 g (59%) of the desired alkyne. ¹H NMR (CDCl₃) δ: 7.53 (br s, 1H); 7.43 (d, 2H); 7.42 (d, 2H); 4.80 (m, 1H); 4.43 (d, 1H); 4.40 (d, 1H); 3.83 (m, 1H); 3.59 (m, 1H); 1.7 (m, 6H).

Part C. Preparation of 3-cyanobenzaldehyde oxime.

Hydroxylamine hydrochloride (13.5 g, 194 mmol) was added to a solution of 3-cyanobenzaldehyde (25 g, 191 mmol) in 75 mL of pyridine and 75 mL of ethanol under N₂. This was allowed to stir at room temperature for 14 hours. Water (50 mL) was added with vigorous stirring and an off-white solid precipitated. The solid was filtered through a glass frit and washed with another 50 mL of water. Evaporation of residual water under high vacuum gave 19.2 g (69%) of title compound. ¹H NMR (CDCl₃) δ: 11.61 (s, 1H); 8.21 (s, 1H); 8.00 (s, 1H); 7.96 (d, 1H), 7.85 (d, 1H), 7.61 (t, 1H).

Part D. Preparation of N-(4-bromophenyl)-3-(3-cyanophenyl)-5-(tetrahydropyran-2-yloxymethyl)-isoxazo-4-yl-carboxamide and N-(4-bromophenyl)-3-(3-cyanophenyl)-4-(tetrahydropyran-2-yloxymethyl)-isoxazo-5-yl-carboxamide.

To a solution of 2.54 g (17.2 mmol) of 3-cyanobenzaldehyde oxime and 7.10 g (21.0 mmol) of N-(4-bromophenyl)-4-(tetrahydropyran-2-yloxymethyl)-2-butynamide in 58 mL THF was added 45 mL bleach (0.67M aqueous solution) over a 4-hour period. The solvent was removed in vacuo and the resulting aqueous solution was extracted with 25 mL EtOAc three times. The combined organic extracts were dried with MgSO₄ and the solvent removed in vacuo. Chromatography on silica with 20% EtOAc/hexane gave 1.4 g (17%) of N-(4-bromophenyl)-3-(3-cyanophenyl)-5-(tetrahydropyran-2-yloxymethyl)isoxazo-4-yl-carboxamide and 1.67 g (20%) of N-(4-bromophenyl)-3-(3-cyanophenyl)-4-(tetrahydropyran-2-yloxymethyl)-isoxazo-5-yl-carboxamide. ¹H NMR (CDCl₃) δ: 1st isomer: 9.45 (br s, 1H); 8.11 (s, 1H); 8.04 (d, 1H); 7.77 (d, 1H); 7.58 (t, 1H); 7.50 (m, 4H); 4.98 (dd, 2H); 4.88 (m, 1H); 3.72 (m, 1H); 3.58 (m, 1H); 1.7 (m, 6H). 2nd isomer: 8.66 (br s, 1H); 8.31 (m, 1H); 8.14 (d, 1H); 7.95 (d, 1H); 7.75 (t, 1H), 7.57 (m, 4H); 4.94 (dd, 2H); 4.87 (m, 1H); 3.87 (m, 1H); 3.57 (m, 1H); 1.6 (m, 6H).

Part E. Preparation of 4-(N-[2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl)-3-(3-cyanophenyl)-5-(tetrahydro-pyran-2-yloxymethyl)-isoxazole.

A mixture of 0.31 g (0.60 mmol) of N-(4-bromophenyl)-3-(3-cyanophenyl)-5-(tetrahydropyran-2-yloxymethyl)isoxazo-4-yl-carboxamide, 0.23 g (0.90 mmol) of 2-(t-butylaminosulfonyl)phenylboronic acid, 0.052 g (0.045 mmol) of tetrakis(triphenylphosphine palladium(0), 0.05 mL of 40% aqueous tetrabutylammonium hydroxide, and 0.9 mL of 2M aqueous sodium carbonate were refluxed with 8 mL of toluene under N₂ for 5.5 hours. After cooling, the mixture was separated and the aqueous layer was extracted with 5 mL of ethyl acetate twice. The combined organic extracts were dried with MgSO₄ and concentrated. The resulting solid was chromatographed with 50% EtOAc/hexane to give 0.27 g (73%) of the desired product. ¹H NMR (CDCl₃) δ: 9.57 (br s, 1H); 8.15 (m, 2H); 8.07 (d, 1H); 7.77 (d, 1H); 7.71 (d, 2H); 7.60 (t, 1H); 7.52 (m, 3H); 7.31 (m, 2H); 5.02 (dd, 2H); 4.94 (m, 1H); 3.72 (m, 1H); 3.60 (m, 1H); 1.7 (m, 6H); 1.04 (s, 9H).

Part F. Preparation of 4-[2′-aminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl-3-(3-cyanophenyl)-5-(hydroxymethyl)-isoxazole.

A solution of 0.27 g (0.56 mmol) of 4-(N-[2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl)-3-(3-cyanophenyl)-5-(tetrahydropyran-2-yloxymethyl)isoxazole in 10 mL of trifluoroacetic acid is allowed to stir under N₂ for 16 hours at room temperature. The solvent was removed in vacuo and then chromatographed on silica with 50% EtOAc/hexane to give 0.11 g (51%) of desired product. ¹H NMR (CDCl₃) δ: 9.19 (br s, 1H); 8.12 (d, 1H); 8.05 (m, 1H); 7.99 (d, 1H); 7.81 (d, 1H); 7.64 (t, 1H); 7.58 (m, 3H); 7.50 (m, 1H); 7.42 (d, 2H); 7.31 (d, 1H); 6.77 (m, 1H); 5.03 (d, 2H). HRMS 475.1076 (M+H).

Part G. Preparation of 3-(3-amidinophenyl)-4-[2′-aminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl-5-(hydroxy-methyl)-isoxazole, trifluoroacetic acid salt.

4-(N-[2′-aminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl)-3-(3-cyanophenyl)-5-(hydroxymethyl)isoxazole (0.11 g, 0.22 mmol) was dissolved in 5 mL of methanol and 10 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 30 minutes to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was added to 0.5 g (5.2 mmol) of ammonium carbonate and 10 mL of methanol. The mixture was allowed to stir under N₂ for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.07 g (53%) of the desired salt. ¹H NMR (DMSO-d₆) δ: 10.60 (s, 1H); 9.43 (br s, 2H); 9.00 (br s, 2H); 8.14 (m, 1H); 7.98 (d, 2H); 7.89 (d, 1H); 7.75 (t, 1H); 7.58 (m, 4H); 7.34 (d, 2H); 7.28 (m, 1H); 4.79 (s, 2H). HRMS 492.1341 (M+H).

Example 2 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

Part A. Preparation of 3-cyanobenzenehydroximinoyl chloride.

3-Cyanobenzaldehyde oxime (15 g, 103 mmol) was suspended in 90 mL of DMF and then N-chlorosuccinimide (13.7 g, 103 mmol) was added. Approximately 50 mL of gaseous HCl was added via syringe below the liquid surface over a 2 minute period. The reaction was allowed to stir at room temperature for 15 hours and the solution clarified. The solvent was evaporated at 5 torr with a bath temp of 55° C. till viscous and cloudy. Water (100 mL) was added with vigorous stirring. An off-white precipitate formed, was filtered through a glass frit and washed with 50 mL water to give 18.1 g (98%) of the desired product after drying under high vacuum. ¹H NMR (CDCl₃) δ: 8.75 (s, 1H), 8.17 (s, 1H), 8.10 (d, 1H), 7.73 (d, 1H), 7.55 (dd, 1H).

Part B. Preparation of 2′-t-butylaminosulfonyl-4-amino-[1,1′]biphenyl.

A mixture of 3.44 g (20 mmol) of 4-bromoaniline and 5.14 g (20 mmol) of 2-(t-butylaminosulfonyl)phenylboronic acid, 1.16 g of tetrakis(triphenylphosphine) palladium(0) (1 mmol), 0.32 g of tetrabutylammonium bromide (1 mmol) and 20 mL of 2M aqueous sodium carbonate were refluxed with 180 mL of benzene under N₂ for 5.5 hours. After cooling, the mixture was diluted with methylene chloride and water. The two phases were separated and the organic phase was washed with water, dried with MgSO₄ and concentrated in vacuo. The resulting thick oil was chromatographed on silica with 30% EtOAc/hexane to afford 2.52 g (41%) of the title compound. ¹H NMR (CDCl₃) δ: 8.14 (d, 1H); 7.53 (t, 1H); 7.43 (t, 1H); 7.33 (d, 2H); 7.27 (d, 1H); 6.76 (d, 2H); 3.7 (br s, 1H); 0.99 (s, 9H.

Part C. Preparation of 3-(3-cyanophenyl)-5-carbomethoxy-isoxazole.

Triethylamine (1.01 g, 10 mmol) is added dropwise over 2 hours to a solution of 0.72 g (4.0 mmol) of 3-cyanobenzenehydroximinoyl chloride and 0.56 g (4.8 mmol) of methyl methoxyacrylate in 10 mL of CH₂Cl₂ under N₂. The reaction mixture is diluted with 10 mL of water and the organic layer separated. The aqueous solution is extracted with 10 mL EtOAc twice and the combined organic extracts are dried with MgSO₄ and concentrated in vacuo. The resulting thick oil was chromatographed on silica with 30% EtOAc/hexane to give 0.90 g (99%) of the desired product. ¹H NMR (CDCl₃) δ: 9.07 (s, 1H); 8.14 (s, 1H); 8.06 (d, 1H); 7.79 (d, 2H); 7.61 (t, 1H); 3.88 (s, 3H).

Part D. Preparation of 3-(3-cyanophenyl)-isoxazole-5-carboxylic acid.

A mixture of 0.90 g (3.9 mmol) of 4-carbomethoxy-3-(3-cyanophenyl)isoxazole, 0.25 g (6.0 mmol) of lithium hydroxide monohydrate in 1 mL water and 2 mL methanol is stirred under N₂ for 5 hours. The reaction mixture was acidified to pH 3 with 1N HCl, extracted with 10 mL EtOAc three times, dried with MgSO₄ and concentrated in vacuo to give 0.36 g (43%) of the desired acid. ¹H NMR (CDCl₃) δ: 8.94 (s, 1H); 8.01 (s, 1H); 7.94 (d, 1H); 7.60 (d, 2H); 7.43 (t, 1H).

Part E. Preparation of 4-(N-[2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl)-3-(3-cyanophenyl)-isoxazole.

Thionyl chloride (10 mL) and 3-(3-cyanophenyl)isoxazole-4-carboxylic acid (0.34 g , 1.6 mmol) are stirred at room temperature under N₂ for 1 hour. The excess thionyl chloride is removed in vacuo and the resulting. solid is resuspended in 10 mL toluene. The toluene is removed in vacuo to remove any residual thionyl chloride. The solid is dissolved in 15 mL CH₂Cl₂ and 0.53 g (1.8 mmol) of 2′-t-butylaminosulfonyl-4-amino-[1,1′]biphenyl and 0.32 g (3.2 mmol) of triethylamine are added. After 2 hours, the reaction mixture is diluted with 10 mL of water and the organic layer separated. The aqueous solution is extracted with 10 mL EtOAc three times and the combined organic extracts are dried with MgSO₄ and concentrated in vacuo. The resulting thick oil was chromatographed on silica with 25% EtOAc/hexane to 0.53 g (66%) of the desired product. ¹H NMR (CDCl₃) δ: 9.07 (s, 1H); 8.14 (m, 1H); 8.06 (m, 1H); 7.81 (d, 1H); 7.55 (m, 9H); 1.03 (s, 9H).

Part F. Preparation of 3-(3-amidinophenyl)-4-[2′-aminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl-5-(hydroxymethyl)-isoxazole, trifluoroacetic acid salt.

4-(N-[2′-aminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl)-3-(3-cyanophenyl)isoxazole (0.53 g, 1.1 mmol) was dissolved in 10 mL of methanol and 30 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 30 minutes to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was added to 0.5 g (5.2 mmol) of ammonium carbonate and 20 mL of methanol. The mixture was allowed to stir under N₂ for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.09 g (15%) of the title salt. ¹H NMR (DMSO-d₆) δ: 10.69 (s, 1H); 9.44 (br s, 2H); 9.06 (br s, 2H); 8.17 (m, 1H); 8.06 (d, 1H); 8.00 (d, 1H); 7.92 (d, 1H); 7.75 (t, 1H); 7.67 (d, 2H); 7.56 (m, 2H); 7.33 (d, 2H); 7.28 (m, 1H). HRMS 462.1252 (M+H).

Example 3 3-(3-amidinophenyl)-4-[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

Part A. Preparation of 2-methylthiophenylboronic acid

2-Bromothioanisole (8.56 g, 42 mmol) was dissolved in 90 mL of dry THF and cooled to −78° C. n-Butyllithium (18.6 mL, 2.5M in hexane, 47 mmol) was added dropwise over 20 minutes, and the resulting solution stirred 90 min. Triisopropylborate (13.7 mL, 59 mmol) was added dropwise over 10 minutes, and the resulting solution stirred at −78° C. for 45 minutes before removing the cooling bath. The reaction was stirred overnight at room temperature. HCl (40 mL of a 6M aqueous solution) was added and stirred vigorously 8 h. The reaction was diluted with 100 mL water and extracted three times with Et₂O. The organic extracts were combined and extracted twice with 80 mL of 2M NaOH. The basic layers were combined and acidified with 50 mL 6M HCl and 25 ml 2M HCl. The resulting cloudy solution was extracted three times with 50 mL of Et₂O, dried over MgSO₄, filtered, and evaporated to yield a white solid (5.22 g, 74%). ¹H NMR (CDCl₃) δ: 8.01 (dd, 1H), 7.53 (dd, 1H), 7.43 (td, 1H), 7.34 (td, 1H), 6.22 (s, 2H), 2.50 (s, 3H).

Part B. Preparation of 4-(t-butoxycarbonyl)amino-2′-methylthio-[1,1′]biphenyl

2-Methylthiophenylboronic acid (5.2 g, 31 mmol), N-t-butylcarbonyl-4-bromoaniline (4.0 g, 15 mmol), Na₂CO₃ (31 mL, 2M aqueous), tetrabutylammonium bromide (230 mg, 0.7 mmol), and bis(triphenylphosphine)palladium(II)chloride (515 mg, 0.7 mmol) were combined in 300 mL of benzene, placed briefly under vacuum to degas, and heated at reflux under argon overnight. The reaction was cooled to room temperature and diluted with 100 mL water and 100 mL EtOAc. The organic layer was separated, dried over Na₂SO₄, filtered through celite, and the solvents evaporated. The crude mixture was chromatographed on silica with 10-30% EtOAc/hexane to yield the desired compound (4.17 g, 90%). ¹H NMR (CDCl₃) δ: 7.42 (d, 2H), 7.35 (d, 2H), 7.28 (m, 2H), 7.19 (m, 2H), 6.53 (bs, 1H), 2.36 (s, 3H), 1.53 (s, 9H).

Part C. Preparation of 4-(t-butoxycarbonyl)amino-2′-methylsulfonyl-[1,1′]biphenyl

4-(t-Butoxycarbonyl)amino-2′-methylthio-[1,1′]biphenyl (4.16 g, 13 mmol) was dissolved in 400 mL of CH₂Cl₂ and cooled to 0° C. MCPBA (11.2 g 57-86%, 37 mmol min.) was added in 4 portions and stirred 25 minutes before removing the cooling bath. The reaction was stirred at room temp for 3 hours. The reaction mixture was then extracted with 50 mL saturated aqueous Na₂SO₃ and then with 50 mL saturated aqueous NaHCO₃. The organic layer was removed, dried over Na₂SO₄, filtered, and evaporated to yield the desired product (4.80 g). ¹H NMR (CDCl₃) δ: 8.22 (dd, 1H), 7.63 (td, 1H), 7.54 (td, 1H), 7.41 (m, 5H), 6.61 (s, 1H), 2.64 (s, 3H), 1.54 (s, 9H).

Part D. Preparation of 4-amino-2′-methylsulfonyl-[1,1′]biphenyl

4-(t-butoxycarbonyl)amino-2′-methylsulfonyl-[1,1′]biphenyl (4.6 g, 13 mmol), was suspended in 100 mL of 4M HCl in dioxane and stirred 2.5 days. The resulting mixture was filtered and the cake rinsed with Et₂O to yield a tan solid (3.69 g, 98%). ¹H NMR (DMSO-d₆) 8.04 (d, 1H), 7.71 (t, 1H), 7.61 (t, 1H), 7.31 (m, 3H), 7.06 (m, 2H), 2.79 (5, 3H).

Part E. Preparation of 3-(3-cyanophenyl)-4-[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole

4-Amino-2′-methylsulfonyl-[1,1′]biphenyl (0.50 g, 2.2 mmol) was suspended in 10 mL of CH₂Cl₂ and 4.4 mL of a 2M solution of trimethylaluminum in heptane was added slowly via syringe. The reaction was stirred for 30 minutes at room temperature and then 3-(3-cyanophenyl)-5-carbomethoxyisoxazole (0.62 g, 2.2 mmol) was added. The reaction mixture was stirred at room temperature for an additional 14 hours. The aluminum reagent was quenched by careful addition of 1N HCl to pH 2, then extracted with 10 mL of CH₂Cl₂ three times. The combined organic extracts were washed with water then brine, dried over MgSO₄ and the solvent evaporated. The desired product was obtained (0.74 g, 76%) after silica gel chromatography with 30% EtOAc/hexane. ¹H NMR (CDCl₃) δ: 9.07 (s, 1H); 8.31 (s, 1H); 8.21 (d, 1H); 8.09 (s, 1H); 8.07 (d, 1H); 7.79 (d, 1H); 7.63 (m, 4H); 7.42 (d, 2H); 7.37 (d, 1H); 2.72 (s, 3H).

Part F. Preparation of 3-(3-amidinophenyl)-4-[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

3-(3-Cyanophenyl)-4-[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole (0.74 g, 1.7 mmol) was dissolved in 10 mL of methanol and 40 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 1.5 hours to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was added to 0.66 g (8.5 mmol) of ammonium carbonate and 20 mL of methanol. The mixture was sealed and allowed to stir under Ar for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.33 g (43%) of the desired salt. ¹H NMR (DMSO-d₆) δ: 10.69 (s, 1H); 9.67 (s, 1H); 9.41 (br s, 2H); 9.07 (br s, 2H); 8.18 (t, 1H); 8.06 (dt, 2H); 7.92 (d, 1H); 7.72 (m, 5H); 7.38 (s, 1H); 7.36 (d, 2H); 2.80 (s, 3H). HRMS 461.1284 (M+H).

Example 4 3-(3-amidinophenyl)-4-[5-(2-aminosulfonyl)phenylpyrid-2-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole, trifluoroacetic acid salt

Part A. Preparation of 3-(3-cyanophenyl)-5-methoxymethyl-4-carbomethoxyisoxazole

Methyl 4-methoxyacetoacetate (1.6 mL, 12 mmol) was dissolved in 12 mL of 2M sodium methoxide in methanol. 3-Cyanobenzenehydroximinoyl chloride (2.0 g, 11 mmol) was dissolved in 10 mL methanol and added to the basic solution over a 5-hour period via syringe pump. The reaction was quenched with 20 mL of saturated, aqueous ammonium chloride. The mixture was extracted with 30 mL EtOAc three times and the combined organic extracts washed with 10 mL water three times. The resulting solution was dried with MgSO₄, concentrated in vacuo and then chromatographed on silica with 10% Et₂O/benzene to 1.14 g (38%) of a white solid. ¹H NMR (CDCl₃) δ: 7.95 (m, 1H); 7.92 (dd, 1H); 7.98 (dd, 1H); 7.60 (t, 1H); 4.91 (s, 2H); 3.83 (s, 3H); 3.54 (s, 3H).

Part B. Preparation of 2-amino-5-(2-t-butylaminosulfonyl)phenylpyridine

A mixture of 1.55 g (9.0 mmol) of 2-amino-5-bromopyridine and 2.3 g (9.0 mmol) of 2-(t-butylaminosulfonyl)phenylboronic acid, 0.52 g of tetrakis(triphenylphosphine) palladium(0) (0.45 mmol), 0.15 g of tetrabutylammonium bromide (0.45 mmol) and 9 mL of 2M aqueous sodium carbonate were refluxed with 80 mL of benzene under Ar for 5 hours. After cooling, the mixture was diluted with 25 mL of methylene chloride and 25 mL of water. The two phases were separated and the organic phase was washed with water, dried with MgSO₄ and concentrated in vacuo. The resulting thick oil was chromatographed on silica with 50% EtOAc/hexane to afford 1.34 g (49%) of the aniline. ¹H NMR (CDCl₃) δ: 8.18 (d, 1H); 8.07 (m, 1H); 7.70 (dd, 1H) 7.58 (dt, 1H); 7.48 (dt, 1H); 7.28 (d, 1H); 6.56 (d, 1H); 4.62 (br s, 2H); 3.88 (br s, 1H); 1.06 (s, 9H).

Part C. Preparation of 3-(3-cyanophenyl)-4-[5-(2-t-butylaminosulfonyl)phenylpyrid-2-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole

3-(3-cyanophenyl)-5-methoxymethyl-4-carbomethoxyisoxazole (1.12 g, 4.1 mmol) was dissolved in 3 mL of THF and 1 mL water. Lithium hydroxide monohydrate (0.20 g, 4.9 mmol) was added and the reaction stirred at room temperature for 5 hours. The solvent was evaporated in vacuo, 100 mL of water was added and the mixture extracted with 50 mL of EtOAc twice. The combined organic extracts were dried with MgSO₄ concentrated in vacuo to give 0.8 g (75%) of a white solid. The crude carboxylic acid (0.4 g, 1.6 mmol) was dissolved in 1.2 mL of 2.0M oxalyl chloride in CH₂Cl₂ followed by 0.1 mL of DMF. The reaction was allowed to stir at room temperature for 2 hours. The reaction was concentrated under high vacuum for 30 minutes to yield a yellow-orange solid. The crude acid chloride was dissolved in 5 mL CH₂Cl₂. 2-Amino-5-(2-t-butylaminosulfonyl)phenylpyridine (0.51 g, 1.86 mmol) followed by triethylamine (0.65 mL, 4.65 mmol) was added to the crude acid chloride solution. The reaction mixture was allowed to stir at room temperature for 14 hours. The solution was diluted with 50 mL CH₂Cl₂, washed with 25 mL saturated, aqueous NaHCO₃, 25 mL 1M HCl then 25 mL brine. The organic layer was dried with MgSO₄, concentrated in vacuo, and chromatographed on silica with 20% EtOAc/benzene to give 0.10 g (12%) of the desired product. ¹H NMR (CDCl₃) δ: 10.07 (br s, 1H); 8.40 (d, 1H); 8.30 (d, 1H); 8.18 (dd, 1H); 8.09 (m, 1H); 8.02 (dt, 1H); 7.84 (dd, 1H); 7.79 (dt, 1H); 7.60 (m, 3H); 7.28 (dd, 1H); 4.89 (s, 2H); 3.71 (s, 3H); 1.07 (s, 9H).

Part D. Preparation of 3-(3-amidinophenyl)-4-[5-(2-aminosulfonyl)phenylpyrid-2-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole, trifluoroacetic acid salt

3-(3-cyanophenyl)-4-[5-(2-t-butylaminosulfonyl)phenylpyrid-2-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole (0.10 g, 0.18 mmol) was dissolved in 1 mL of methanol and 4 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 2.5 hours to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was added to 0.07 g (0.90 mmol) of ammonium carbonate and 10 mL of methanol. The mixture was sealed and allowed to stir under Ar for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.33 g (43%) of the desired salt. ¹H NMR (DMSO-d₆) δ: 10.69 (s, 1H); 9.67 (s, 1H); 9.41 (br s, 2H); 9.07 (br s, 2H); 8.18 (t, 1H); 8.06 (dt, 2H); 7.92 (d, 1H); 7.72 (m, 5H); 7.38 (s, 1H); 7.36 (d, 2H); 2.80 (s, 3H). HRMS 507.1458 (M+H).

Example 5 3-(3-amidinophenyl)-4-[(2′-trifluoramethyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

Part A. Preparation of 2-(trifluoromethyl)phenylboronic acid

To a solution of 58.8 g (0.261 mol) of 1-bromo-2-(trifluoromethyl)benzene in 250 mL of THF under Ar was added 110 mL (0.275 mol) of 2.5M n-butyllithium in hexane over 35 minutes, keeping the temperature between 0-5° C. The reaction mixture was allowed to warm to 10° C. Triisopropylborate (95 mL, 0.313 mol) was added, keeping the temperature below 35° C. After 1 hour, the reaction mixture was cooled, 1N HCl (425 mL) was added, and the mixture was stirred overnight. The mixture was extracted with 100 mL of ether three times, and the combined organic extracts were extracted with 100 mL of 1N NaOH three times. The aqueous extracts were acidified to pH 1 with 6N HCl, and then extracted with 100 mL ether three times. The combined ether extracts were dried over MgSO₄, and the solvents evaporated in vacuo to give 46.1 g (93%) of the desired compound as a light yellow oil. ¹H NMR (CDCl₃) δ: 7.77 (d, 1H); 7.72 (d, 1H); 7.56 (m, 2H); 4.87 (br s, 2H).

Part B. Preparation of 4-amino-2′-trifluoromethyl-[1,1′]biphenyl

A mixture of 3.44 g (20 mmol) of 4-bromoaniline and 3.80 g (20 mmol) of 2-(trifluoromethyl)phenylboronic acid, 1.16 g of tetrakis(triphenylphosphine) palladium(0) (1 mmol), 0.32 g of tetrabutylammonium bromide (1 mmol) and 20 mL of 2M aqueous sodium carbonate were refluxed with 180 mL of benzene under N₂ for 14 hours. After cooling, the mixture was diluted with methylene chloride and water. The two phases were separated and the organic phase was washed with water, dried with MgSO₄ and concentrated in vacuo. The resulting thick oil was chromatographed on silica with 10% EtOAc/hexane to afford 2.09 g (44%) of the aniline. ¹H NMR (CDCl₃) δ: 7.72 (d, 1H); 7.53 (t, 1H); 7.41 (t, 1H); 7.32 (d, 1H); 7.13 (d, 2H); 6.73 (d, 2H); 3.74 (br s, 2H).

Part C. Preparation of 3-(3-cyanophenyl)-4-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole

4-Amino-2′-trifluoromethyl-[1,1′]biphenyl (0.24 g, 1.0 mmol) was suspended in 5 mL of CH₂Cl₂ and 2.5 mL of a 2M solution of trimethylaluminum in heptane was added slowly via syringe. The reaction was stirred for 30 minutes at room temperature and then 4-carbomethoxy-3-(3-cyanophenyl)isoxazole (0.25 g, 1.0 mmol) was added. The reaction mixture was stirred at room temperature for an additional 14 hours. The aluminum reagent was quenched by careful addition of 1N HCl to pH 2, then extracted with 10 mL of CH₂Cl₂ three times. The combined organic extracts were washed with water then brine, dried over MgSO₄ and the solvent evaporated. The desired product was obtained (0.35 g, 80%) after silica gel chromatography with 20% EtOAc/hexane. ¹H NMR (CDCl₃) δ: 9.02 (s, 1H); 8.17 (s, 1H); 8.08 (d, 1H); 7.83 (d, 1H); 7.76 (d, 1H); 7.67 (t, 1H); 7.56 (m, 1H); 7.48 (m, 3H); 7.34 (m, 3H).

Part D. Preparation of 3-(3-amidinophenyl)-4-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

3-(3-cyanophenyl)-4-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole (0.33 g, 0.76 mmol) was dissolved in 1 mL of methanol and 3 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 0.5 hours to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was added to 0.25 g (2.6 mmol) of ammonium carbonate and 2 mL of methanol. The mixture was sealed and allowed to stir under Ar for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.11 g (32%) of the desired salt. ¹H NMR (DMSO-d₆) δ: 10.68 (s, 1H); 9.68 (s, 1H); 9.43 (br s, 2H); 9.06 (br s, 2H); 8.20 (m, 1H); 8.08 (d, 1H); 7.93 (d, 1H); 7.75 (m, 5H); 7.60 (d, 1H); 7.38 (m, 1H); 7.31 (d, 2H). HRMS 451.1399 (M+H).

Example 6 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(trifluoramethyl)isoxazole, trifluoroacetic acid salt

Part A. Preparation of ethyl 3-methoxy-3-(trifluoromethyl)acylate

Diazald® (14.55, 67.9 mmol) was dissolved in 130 mL Et₂O and 30 mL 95% EtOH. Potassium hydroxide (12.37 g, 220 mmol) is dissolved in 23 mL water and added slowly via additional funnel to the ethanol solution which is heated to 65° C. The ether distillate containing diazomethane is condensed into ethyl 4,4,4-trifluoroacetoacetate (10.0 g, 54.3 mmol). The excess diazomethane was decomposed with the addition of 1 drop of acetic acid. The ethereal solution was evaporated at 450 torr for 30 minutes. The crude enol ether (10.7 g, 100%) was used without purification. ¹H NMR (CDCl₃) δ: 5.78 (s, 1H); 4.22 (q, 2H); 4.04 (s, 3H); 1.32 (t, 3H).

Part B. Preparation of 3-(3-cyanophenyl)-5-(trifluoromethyl-4-carbomethoxyisoxazole

Tributylamine (12.6 g, 67.9 mmol) is added dropwise over 2 hours to a solution of 9.81 g (54.3 mmol) of 3-cyanobenzene-hydroximinoyl chloride and 10.76 g (54.3 mmol) of ethyl 3-methoxy-3-(trifluoromethyl)acylate in 49 mL of CH₂Cl₂ and 1 mL DMSO under N₂. The reaction mixture is diluted with 100 mL of water and the organic layer separated. The aqueous solution is extracted with 100 mL EtOAc twice and the combined organic extracts are dried with MgSO₄ and concentrated in vacuo. The resulting thick oil was chromatographed on silica with 30% EtOAc/hexane to give 1.60 g (10%) of the desired product. ¹H NMR (CDCl₃) δ: 8.05 (m, 1H); 7.96 (dt, 1H); 7.84 (dt, 1H); 7.63 (t, 1H); 4.37 (q, 2H); 1.33 (t, 3H).

Part C. Preparation of 3-(3-cyanophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1]-biphen-4-yl)aminocarbonyl]-5-(trifluoromethyl)isoxazole

2′-t-Butylaminosulfonyl-4-amino-[1,1′]biphenyl (0.39 g, 1.3 mmol) was suspended in 4 mL of CH₂Cl₂ and 1.9 mL of a 2M solution of trimethylaluminum in heptane was added slowly via syringe. The reaction was stirred for 30 minutes at room temperature and then 3-(3-cyanophenyl)-5-(triflouromethyl-4-carbomethoxyisoxazole (0.40 g, 1.3 mmol) was added. The reaction mixture was stirred at room temperature for an additional 14 hours. The aluminum reagent was quenched by careful addition of 1N HCl to pH 2, then extracted with 20 mL of CH₂Cl₂ three times. The combined organic extracts were washed with water then brine, dried over MgSO₄ and the solvent evaporated. The desired product was obtained (0.31 g, 43%) after silica gel chromatography with 20% EtOAc/hexane. ¹H NMR (CDCl₃) δ: 8.74 (br s, 1H); 8.11 (d, 1H); 8.05 (m, 1H); 8.02 (d, 1H); 7.76 (d, 1H); 7.55 (m, 5H); 7.37 (d, 2H); 7.28 (d, 1H); 1.03 (s, 9H).

Part D. Preparation of 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(trifluoromethyl)isoxazole, trifluoroacetic acid salt

3-(3-cyanophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(trifluoromethyl)isoxazole (0.30 g, 0.53 mmol) was dissolved in 1 mL of methanol and 3 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 0.5 hours to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was added to 0.25 g (2.6 mmol) of ammonium carbonate and 2 mL of methanol. The mixture was sealed and allowed to stir under Ar for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.11 g (36%) of the desired salt. ¹H NMR (DMSO-d₆) δ: 11.17 (s, 1H); 9.46 (br s, 2H); 9.09 (br s, 2H); 8.19 (m, 1H); 7.98 (m, 3H); 7.84 (t, 1H); 7.56 (m, 2H); 7.55 (d, 2H); 7.37 (d, 2H); 7.26 (m, 1H). HRMS 586.1743 (M+H).

Examples 7 and 8 2-Acetylamino-4-(3-amidinophonyl)-5-[(2′-aninosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 7) and 2-amino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl) amiinocarbonyl]thiazole, trifluoroacetic acid salt (Example 8)

Part A. Preparation of methyl 3-(3-cyanophenyl)-3-hydroxypropionate.

To a suspension of activated zinc powder (4.3 g, 65.4 mmol) in 100 mL of tetrahydrofuran was added a few drops of dibromoethane. The resulting mixture was heated to 65° C., stirred for 5 min and then was cooled to 25° C. To this solution was added methyl bromoacetate (5.0 g, 32.7 mmol) and 3-cyanobenzaldehyde (4.3 g, 32.7 mmol). The mixture was heated to 65° C. and stirred for 2 h. The reaction was allowed to cool to 25° C. and then was quenched with 10% aq HCl and filtered through celite. The mixture was diluted with ethyl acetate and washed with 10% aq HCl and saturated ag NaHCO₃. This wash cycle was repeated until no white precipitate was observed upon addition of saturated aq NaHCO₃. The organics were then washed with brine, dried (MgSO₄) and concentrated in vacuo. The residue was purified by flash chromatography (elution with 1:1 hexanes/ethyl acetate) to afford 4.5 g (67%) of the title compound as an oil. MS (NH₃-DCI) 223.1 (M+H)+.

Part B. Preparation of methyl 3-(3-cyanophenyl)-3-oxopropionate.

To a solution of methyl 3-(3-cyanophenyl)-3-hydroxypropionate (2.22 g, 10.8 mmol) in 30 mL of methylene chloride was added activated manganese dioxide (4.7 g, 54.0 mmol). This mixture was allowed to stir at 25° C. for 16 h. The reaction mixture was filtered through a pad of celite and concentrated in vacuo. The residue was purified by flash chromatography (elution with 2:1 hexanes/ethyl acetate) to afford 0.9 g (41%) of the title compound along with 0.8 g (36%) of recovered starting material. MS for title compound (H₂OGC-MS) 204 (M+H)+.

Part C. Preparation of methyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate.

To a solution of methyl 3-(3-cyanophenyl)-3-oxopropionate (0.91 g, 4.48 mmol) in 20 mL of carbon tetrachloride at 0° C. was added N-bromosuccinimide (0.80 g, 4.48 mmol). The resulting solution was allowed warm to 25° C. and was stirred for 2 h. The insoluble succinimide was filtered off and the solution was concentrated in vacuo to afford an oil (1.2 g, 95%) which was sufficiently pure to be used without purification. MS (H₂OGC-MS) 282/284 (M+H)+.

Part D. Preparation of 2-acetylamino-4-(3-cyanophenyl)-5-carbomethoxythiazole.

To a solution of methyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (1.25 g, 4.4 mmol) in 20 mL of tetrahydrofuran was added 1-acetylthiourea (0.52 g, 4.4 mmol). The resulting mixture was stirred at 65° C. for 3 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with 10% aq HCl, saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl acetate left the title compound as a white solid (0.4 g, 30%). MS (ESI) 302.2 (M+H)+.

Part E. Preparation of 2-acetylamino-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

To a solution of (2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)amine (0.27 g, 0.88 mmol) in 5 mL of methylene chloride at 25° C. was added trimethylaluminum (1.76 mL of a 2.0 M solution in toluene, 3.52 mmol) dropwise. The resulting solution was allowed to stir until no more gas evolution was observed (˜15 min). To this solution was added 2-acetylamino-4-(3-cyanophenyl)-5-carbomethoxythiazole (0.12 g, 0.40 mmol) as a solution in methylene chloride. The resulting solution was stirred at 40° C. for 2 h and then was cooled to 25° C. and quenched by the addition of saturated aq NH₄Cl. After diluting with ethyl acetate, the organic layer was washed with 10% aq HCl, saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo. The residue was purified by flash chromatography (elution with 1:1 hexanes/ethyl acetate) to afford 0.15 g (65%) of the title compound as a solid. MS (ESI) 574 (M+H)+.

Part F. Preparation of 2-acetylamino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 7) and 2-amino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 8).

Through a solution of 2-acetylamino-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (0.15 g, 0.26 mmol) in 50 mL of absolute methanol at 0° C. was bubbled anhydrous HCl (g) until the solution was saturated. This solution was tightly stoppered and allowed to stand at 0° C. for 16 h. The solution was concentrated in vacuo and then was taken up in 10 mL of absolute methanol and then there was added ammonium carbonate (0.15 g, 1.56 mmol). This mixture was allowed to stir at 25° C. for 16 h. The reaction mixture was then concentrated in vacuo and purified by prep HPLC (C18 reverse phase column, elution with a H₂O/CH₃CN gradient with 0.5% TFA) to afford 2-acetylamino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 7) as the major product (0.50 g, 30%). MS (ESI) 535 (M+H)+. There was also isolated 2-amino-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 8) as a minor product (0.10 g, 6%). MS (ESI) 493 (M+H)+.

Example 9 2-Methyl-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of 2-methyl-4-(3-cyanophenyl)-5-carbomethoxythiazole.

To a solution of methyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate from Example 1, Part C(0.50 g, 1.77 mmol) in 10 mL of tetrahydrofuran was added thioacetamide (0.14 g, 1.77 mmol). The resulting solution was stirred at 65° C. for 4 h and then was allowed to cool to 25° C. This mixture was diluted with ethyl acetate, washed with 10% aq HCl, saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo to a solid. Trituration with ether left 0.14 g (31%) of the title compound as a solid. MS (NH₃-CI) 259 (M+H)+.

Part B. Preparation of 2-methyl-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 1, Part E, 2-methyl-4-(3-cyanophenyl)-5-carbomethoxythiazole (0.08 g, 0.31 mmol) was converted into 0.085 g (52%) of the title compound as a solid. MS (ESI) 531.3 (M+H)+.

Part C. Preparation of 2-methyl-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

A solution of 2-methyl-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (0.085 g, 0.16 mmol) in 5 mL of trifluoroacetic acid was stirred at 70° C. until gas evolution was no longer observed (˜15 min) and then was allowed to cool to room temperature and as concentrated in vacuo. The crude residue was dissolved in 40 mL of absolute methanol and cooled to 0° C. Anhydrous HCl gas was bubbled through the solution until saturated (˜30 min). The flask was then sealed and allowed to stand at 0° C. for 16 h. The reaction mixture was concentrated in vacuo, dissolved in 10 mL of absolute methanol and then ammonium carbonate (0.09 g, 0.96 mmol) was added and the mixture was allowed to stir at 25° C. for 24 h. The reaction mixture was concentrated in vacuo and purified by prep HPLC (C18 reverse phase column, elution with a H₂O/CH₃CN gradient with 0.5% TFA) to afford 65 mg (68%) of the title compound as a solid. MS (ESI) 492.3 (N+H)+.

Example 10 5-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aaminocarbonyl]oxazole

Part A. Preparation of 5-(3-cyanophenyl)-4-carboxymethyloxazole.

The title compound was prepared in 50% yield by the condensation of 3-cyanobenzoyl chloride, methylisocyanoacetate and triethylamine in anhydrous THF following the general method of Suzuki et. al. Syn. Comm. 1972, 2, 237. ¹H NMR (CDCl₃) δ: 8.42-8.40 (d, 1H), 7.99 (s, 1H), 9.77-7.75 (d, 1H), 7.63 (t, 1H), 3.99 (s, 3H) ppm; Ammonia mass spectrum analysis m/z (rel intensity) 246(M+NH₄ ⁺, 100), 229(M+H).

Part B. Preparation of 5-(3-cyanophenyl)-oxazole-4-carboxylic acid.

Standard LiOH hydrolysis in aqueous THF of the product from part A then provided pure oxazole carboxylic acid in quantitative yield. ¹H NMR (CDCl₃) δ: 8.56-8.34 (d, 1H), 8.51 (s, 1H), 8.03 (s, 1H), 7.77-7.76 (d, 1H), 7.67-7.62 (t, 1H) ppm; Ammonia mass spectrum analysis m/z (rel intensity) 232 (M+NH₄ ⁺, 100) ppm.

Part C. Preparation of 5-(3-cyanophenyl)-4-[(2′-t-butyl-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]oxazole.

The acid obtained in part B was then coupled (60% yield) to 2′-tert-butylsulfonamide-biphenylaniline acid chloride as described above. ¹H NMR (CDCl₃) δ: 9.24 (s, 1H), 8.71 (s, 1H), 8.67 (s, 1H), 8.19-8.16 (m, 1H), 8.01 (s, 1H), 7.83-7.80 (d, 2H), 7.76 (m, 1H), 7.67 (d, 1H), 7.35-7.32 (m, 1H), 3.62 (s, 1H), 1.03 (s, 9H) ppm; ESI mass spectrum analysis m/z (rel. intensity) 445 (M+H, 100).

Part D. Preparation of 5-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]oxazole.

The compound obtained in part C was subjected to the Pinner-amidine reaction sequence as outlined previously to obtain the title benzamidine compound in 40% yield. Colorless crystals obtained after lyophilization. ¹H NMR (DMSO d₆) δ: 10.49 (s, 1H), 9.45 (bs, 2H), 9.12 (bs, 2H), 8.85 (s, 1H), 8.61 (s, 1H), 8.54-8.51 (d, 1H), 8.05 (d, 1H), 7.91-7.77 (m, 4H), 7.65-7.54 (m, 2H), 7.40-7.37 (d, 2H), 7.35 (d, 1H), 7.27 (s, 2H) ppm; ESI mass spectrum analysis m/z (rel. intensity) 462 (M+H, 100); High resolution mass spectrum analysis calc. for C₂₃H₂₀N₅SO₄ 462.123601, found 462.124334.

Example 11 3-(3-amidinophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

4-(N-[2′-Aminosulfonyl-[1,1′]-biphen-4-yl]aminocarbonyl)-3-(3-cyanophenyl)isoxazole (0.53 g, 1.1 mmol) was dissolved in 10 mL of methanol and 30 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled for 30 minutes to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was used in the next step.

The imidate formed above was added with 0.5 g (5.2 mmol) of ammonium carbonate and 20 mL of methanol. The mixture was allowed to stir under N₂ for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.09 g (16%) of the desired salt. ¹H NMR (DMSO-d₆) δ: 10.69 (s, 1H); 9.70 (s, 1H); 9.43 (br s, 2H); 9.05 (br s, 2H); 8.05 (d, 1H); 8.00 (d, 1H); 7.92 (d, 1H); 7.74 (t, 1H); 7.67 (d, 2H); 7.59 (t, 1H); 7.52 (t, 1H); 7.34 (d, 2H); 7.26 (m, 1H); 0.98 (s, 9H). HRMS 517.1768 (M+H).

Example 12 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole, trifluoroacetic acid salt

Part A. Preparation of methyl 3-(3-cyanophenyl)-5-(methoxymethyl)isoxazole-4-carboxylate.

Methyl 4-methoxyacetoacetate (1.6 mL, 12.2 mmol) was added to a solution of 12.2 mL (24.4 mmol) of 0.5 M NaOMe in methanol. A solution of 3-cyanobenzenehydroximinoyl chloride (2.0 g, 11.1 mmol) in 20 mL methanol was added slowly over 12 hours vis a syringe pump. The reaction mixture was diluted with 20 mL of saturated aqueous ammonium chloride and the organic layer separated. The aqueous solution was extracted with 10 mL EtOAc twice. The combined organic extracts were washed with 10 mL water three times then the organic extract was dried with MgSO₄ and concentrated in vacuo. The resulting thick oil (3.1 g) was chromatographed on silica with 10% Et₂O/benzene to give 1.14 g (38%) of the desired product. ¹H NMR (CDCl₃) δ: 7.98 (m, 1H); 7.91 (dd, J=8.1, 2.9, 1H); 7.79 (dd, J=8.1, 2.9, 1H); 7.59 (t, J=8.1, 1H); 4.91 (s, 2H); 3.83 (s, 3H); 3.53 (s, 3H) MS (NH₃-CI) m/z 273.0 (M+H).

Part B. Preparation of 3-(3-cyanophenyl)-5-(methoxymethyl)-isoxazole-4-carboxylic acid.

Methyl 3-(3-cyanophenyl)-5-(methoxymethyl)isoxazole-4-carboxylate (1.12 g, 4.1 mmol) was dissolved in 3 mL THF and 1 mL water. Lithium hydroxide monohydrate (0.20 g, 4.9 mmol) was added and the reaction was allowed to stir for 24 hours under N₂. The solvent was removed in vacuo and redissolved in 100 mL of water. The resulting solution was extracted with 30 mL EtOAc twice then acidified with 1N HCl to pH 3. The acidic solution was extracted three times with 30 mL of EtOAc. The combined organic were dried with MgSO₄ and concentrated in vacuo to give the desired white solid (0.80 g, 75%). ¹H NMR (CDCl₃) δ: 7.98 (m, 1H); 7.91 (dd, J=8.1, 2.9, 1H); 7.79 (dd, J=8.1, 2.9, 1H); 7.59 (t, J=8.1, 1H); 4.89 (s, 2H); 3.53 (s, 3H).

Part C. Preparation of 3-(3-cyanophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole.

Oxalyl chloride (1.15 mL of 2.0 M solution in CH₂Cl₂, 2.3 mnmol) and 3-(3-cyanophenyl)-5-(methoxymethyl)isoxazole-4-carboxylic acid (0.40 g, 1.55 mmol) were stirred at room temperature under N₂ for 1 hour. The excess oxalyl chloride was removed in vacuo. The solid was dissolved in 15 mL CH₂Cl₂ and 0.58 g (1.9 mmol) of 2′-t-butylaminosulfonyl-4-amino-[1,1′]-biphenyl and 0.65 mL (4.7 mmol) of triethylamine were added. After 12 hours, the reaction mixture was diluted with 10 mL of water and the organic layer separated. The aqueous solution was extracted with 10 mL CH₂Cl₂ three times and the combined organic extracts were washed with 10 mL of each of the following: saturated aqueous NaHCO₃, 1M aqueous HCl and saturate aqueous brine. The organic extract was dried with MgSO₄ and concentrated in vacuo to give 0.63 g of an orangebrown solid. The solid was chromatographed on silica with 10% EtOAc/benzene to 0.63 g (74%) of the desired product. ¹H NMR (CDCl₃) δ: 9.50 (s, 1H); 8.16 (d, J=8.1, 1H); 8.11 (s, 1H); 8.04 (d, J=8.1, 1H); 7.78 (d, J=8.1, 1H); 7.66 (d, j=8.8, 2H); 7.60 (m, 1H); 7.56 (m, 2H); 7.50 (d, J=8.8, 2H); 7.29 (d, J=7.3, 1H); 4.89 (s, 2H); 3.67 (s, 3H); 1.03 (s, 9H).

Part D. Preparation of 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole, trifluoroacetic acid salt.

3-(3-Cyanophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole (0.62 g, 1.14 mmol) was dissolved in 7 mL of methanol and 20 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 1.5 hours to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was used in the next step.

The imidate formed above was added with 0.44 g (5.7 mmol) of ammonium carbonate and 20 mL of methanol. The mixture was allowed to stir under N₂ for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.37 g (65%) of the desired salt. ¹H NMR (DMSO-d₆)δ: 10.63 (s, 1H); 9.42 (s, 1H); 9.03 (br s, 2H); 9.05 (br s, 2H); 8.16 (s, 1H); 8.00 (m, 1H); 7.98 (m, 1H); 7.90 (d, J=7.3, 1H); 7.76 (t, J=8.1, 1H); 7.57 (m, 4H); 7.34 (d, J=8.1, 2H); 7.28 (m, 1H); 4.77 (s, 2H); 3.34 (s, 3H). HRMS 506.1487 (M+H).

Example 13 2-Methyl-4-(3-amidinophenyl)-5-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of 2-methyl-4-(3-cyanophenyl)-5-[4-bromophenyl)aminocarbonyl]thiazole.

To a solution of 4-bromoaniline (0.21 g, 1.2 mmol) in 25 mL of methylene chloride at room temperature was added trimethylaluminum (1.02 mL of a 2.0M solution in toluene, 2.04 mmol) dropwwase. The reaction was stirred until gas evolution ceased and then 2-methyl-4-(3-cyanophenyl)-5-carbomethoxythiazole from Example 3, Part A (0.26 g, 1.02 mmol) was added in 10 mL of methylene chloride. The resulting solution was stirred at 40° C. for 16 h and then was allowed to cool to 25° C. This mixture was quenched with saturated aq NH₄Cl, diluted with ethyl acetate, washed with water and brine, dried (MgSO₄) and concentrated in vacuo. The residue was purified by flash chromatography (elution with 4:1 hexanes/ethyl acetate) to afford 0.18 g (44%) of the title compound as a solid. MS (ESI) 398.0/400.0 (M+H)+.

Part B. Preparation of 2-methyl-4-(3-cyanophenyl)-5-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

To a solution of 2-methyl-4-(3-cyanophenyl)-5-[4-bromophenyl)aminocarbonyl]thiazole (0.175 g, 0.44 mmol) in 25 mL of benzene was added 2-(trifluoromethyl)phenylboronic acid (0.118 g, 0.62 mmol); tetrabutylammonium bromide (0.006 g, 0.02 mmol); sodium carbonate (0.14 g, 1.3 mmol) and 1.2 mL of H₂O. This mixture was degassed with a stream of nitrogen and then tetrakis(triphenylphosphine)palladium (0.02 g, 0.02 mmol) was added and the reaction mixture was stirred at 80° C. for 16 h. The mixture was allowed to cool to room temperature and then was diluted with ethyl acetate, washed with H₂O and brine, dried over MgSO₄ and was concentrated in vacuo to afford 0.166 g (83%) of the title compound, which was sufficiently pure to be used without purification. MS (ESI) 464.2 (M+H)+.

Part C. Preparation of 2-methyl-4-(3-amidinophenyl)-5-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Following the procedure described in Example 7, Part F, 2-methyl-4-(3-cyanophenyl)-5-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (0.166 g, 0.36 mmol) was converted into 45 mg (21%) of the title compound as a white solid following HPLC purification. MS (ESI) 481.3 (M+H)+.

Example 14 2-Phenyl-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of 2-phenyl-4-(3-cyanophenyl)-5-carbomethoxythiazole.

To a solution of methyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate from Example 7, Part C (0.51 g, 1.8 mmol) in 20 mL of absolute ethanol was added thiobenzamide (0.25 g, 1.8 mmol). The resulting mixture was stirred at 80° C. for 24 h. The reaction was allowed to cool and then was filtered. The solid was washed with ethanol and dried in vacuo to yield 0.53 g (91%) of the title compound. MS (ESI) 321.1 (M+H)+.

Part B. Preparation of 2-phenyl-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-phenyl-4-(3-cyanophenyl)-5-carbomethoxythiazole (0.30 g, 0.94 mmol) was converted into 0.53 g (95%) of the title compound as a solid. MS (ESI) 593.3 (M+H)+.

Part C. Preparation of 2-phenyl-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Following the procedure of Example 9, Part C, 2-phenyl-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (0.53 g, 0.90 mmol) was converted into 61 mg of the title compound (10%) as a white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 10.77 (s, 1H), 9.40 (broad s, 2H), 8.98 (broad s, 2H), 8.28 (broad s, 1H), 8.08 (m, 3H), 7.99 (d, 1H, J=8 Hz), 7.81 (d, 1H, J=8 Hz), 7.71 (t, 1H, J=8 Hz), 7.61-7.52 (m, 7H), 7.38-7.22 (m, 5H). MS (ESI) 554.3 (M+H)+.

Example 15 3-(3-amidinophenyl)-4-[(3-fluoro-2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

Part A. Preparation of 3-fluoro-2′-methylthio-[1,1′]-biphenylamine.

A benzene solution (100 mL) of 2-methylthiophenylboronic acid (2.07 g, 12.3 mmol); 4-bromo-2-fluoro aniline (1.06 g, 5.6 mmol); aq. Na₂CO₃ (12.5 mL, 2 M, 25 mmol); and tetra n-butyl ammonium bromide (90 mg, 0.3 mmol) was purged with vacuum and Ar. Bis(triphenylphosphine)palladium (II) chloride (195 mg, 0.3 mmol) was added, and the reaction was refluxed 10 h. After cooling, the reaction was diluted with EtOAc and H₂O, the layers were separated, the organic was dried over Na₂SO₄, filtered, and evaporated. The crude product was chromatographed on silica gel (10% EtOAc/hexanes) to yield the desired product (1.05 g, 81%). H NMR (CDCl₃) δ: 7.29 (m, 2H); 7.18 (m, 2H); 7.09 (dd, 1H, J=11.7, J′=1.8); 7.01 (dd, 1H, J=8.0, J′=1.4); 6.82 (t, 1H, J=9.2); 3.79 (bs, 2H); 2.38 (s, 3H).

Part B. Preparation of 3-(3-cyanophenyl)-4-[(3-fluoro-2′-methylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole.

Trimethyl aluminum (1.3 mL, 2.0 M in heptane, 2.6 mmol) was added to the 4-amino-3-fluoro-2′-methylthio-[1,1′]-biphenyl (309 mg, 1.3 mmol) in CH₂Cl₂ (7 mL) and stirred at room temp 25 min. Then methyl 3-(3-cyanophenyl)isoxazole-4-carboxylate isoxazole (300 mg, 1.3 mmol) was added and stirred 48 h. More trimethyl aluminum (1.3 mL, 2.6 mmol) and CH₂Cl₂ (5 mL) were added. After an additional 3 days, the reaction was quenched carefully with 1N HCl and extracted into CH₂Cl₂. The organic layer was further washed with H₂O and brine, dried over Na₂SO₄, filtered, and evaporated. The crude produc was chromatographed on silica gel (20-30% EtOAc/hexanes followed by 2%MeOH/CHCl₃) to yield the desired product (0.50 g, 89%). ¹H NMR (CDCl_(3, 400) MHz) δ: 9.07 (s, 1H); 8.34 (bt, 1H, J=8.3); 8.13 (t, 1H, J=1.2); 8.04 (dt, 1H, J=7.8, J′=1.2); 7.84 (dt, 1H, J=7.8, J′=1.4); 7.67 (t, 1H, J=8.1); 7.57 (bs, 1H); 7.35 (m, 1H); 7.28 (m, 1H); 7.19 (m, 4H); 2.38 (s, 1H).

Part C. Preparation of 3-(3-cyanophenyl)-4-[(3-fluoro-2′-methylsulfonyl-[1,1]-biphen-4-yl)aminocarbonyl]isoxazole.

To a chloroform solution (50 mL) of 3-(3-cyanophenyl)-4-[(3-fluoro-2′-methylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole (0.47 g, 1.1 mmol); m-CPBA (351 mg, 57-86%, max 1.7 mmol) was added. The resulting mixture was stirred at room temp under Ar 22 h. Additional m-CPBA (94 mg of 50-60% and 348 mg of 57-86%, max 2.1 mmol) was added and stirred 4 h. The reaction was extracted with sat. aq. Na₂SO₃ and sat. NaHCO₃, dried over Na₂SO₄, filtered, and evaporated. The crude product was chromatographed on silica gel (30-50% EtOAc/hexanes) to yield the desired sulfone (447 mg, 88%). ¹H NMR (CDCl₃) δ: 9.10 (s, 1H); 8.41 (t, 1H, J=8.4); 8.22 (dd, 1H, J=7.7, J′=1.5); 8.12 (d, 1H, J=1.5); 8.05 (dt, 1H, J=8.1, J′=1.5); 7.86 (dt, 1H, J=7.7, J′=1.5); 7.64 (m, 4H); 7.28 (m, 3H); 2.73 (s, 3H).

Part C. Preparation of 3-(3-amidinophenyl)-4-[(3-fluoro-2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt.

Solid 3-(3-cyanophenyl)-4-[(3-fluoro-2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole (423 mg, 0.92 mmol) was suspended in methanol (15 mL) and cooled to 0° C. HCl (g) was generated by the addtion of conc. H₂SO₄ (90 mL) into solid NaCl (360 g) over 1 h. The HCl (g) continued bubbling through the reaction an additional 90 min, at which time the generator and ice bath were removed. The reaction stirred under argon 20 h and was evaporated. After a few hours under high vacuum, the reaction was redissolved in methanol (15 mL); and ammonium carbonate (440 mg, 4.6 mmol) was added. The reaction was stirred 22 h and evaporated. The crude product was purified by prep HPLC on a C-18 reverse phase column (20-80% MeCN/H₂O/0.05% TFA) to yield a white solid (0.14 g, 26%). ¹H NMR (DMSO-d₆)δ: 10.47 (s, 1H); 9.68 (s, 1H); 9.40 (s, 1.5H); 9.01 (s, 1.5 H); 8.16 (s, 1H); 8.06 (m, 2H); 7.91 (d, 1H, J=8.1); 7.72 (m, 4H); 7.37 (m, 2H); 7.21 (d, 1H, J=8.1); 2.90 (s, 3H). HRMS calc. for C₂₄H₂₀FN₄O₄S, 479.1189; found, 479.1169.

Example 16 3-(3-amidinophenyl)-4-[(2′-trifluoromethylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

Part A. Preparation of 3-(3-cyanophenyl)-4-[(2′-trifluoromethylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole.

Trimethyl aluminum (2.6 mL, 2.0 M in heptane, 5.2 mmol) was added to the 4-amino-2′-trifluoromethylthio-[1,1′]-biphenyl (361 mg, 1.3 mmol); in CH₂Cl₂ (5 mL) and stirred at room temp 8 min. A CH₂Cl₂ solution (5 mL) of methyl 3-(3-cyanophenyl)isoxazole-4-carboxylate (300 mg, 1.3 mmol) was added and stirred 2 days. No further reaction was observed after adding more trimethyl aluminum (650 mL) and stirring an additional 20 hr. The reaction was quenched cwerefully with 1 M HCl and extracted into CH₂Cl₂. The organic was extracted again with water and brine, dried over Na₂SO₄, filtered, and evaporated. The crude mixture was chromatographed on silica gel (30% EtOAc/hexanes) to yield a yellow solid (565 mg, 92%). ¹H NMR (CDCl₃) δ: 9.02 (s, 1H); 8.17 (s, 1H); 8.09 (d, 1H, J=8.1); 7.82 (t, 2H, J=8.1); 7.66 (t, 1H, J=7.7); 7.53 (m, 4H); 7.42 (t, 2H, J=7.7); 7.32 (d, 2H, J=8.4).

Part B. Preparation of 3-(3-amidinophenyl)-4-[(2′-trifluoromethylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole.

A methanol solution (10 mL) of 3-(3-cyanophenyl)-4-[(2′-trifluoromethylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole (137 mg, 0.29 mmol) was cooled to 0° C. HCl was generated by the slow addition of conc. H₂SO₄ (60 mL) to solid NaCl (240 g) over 1 h. The HCl thus generated was bubbled into the reaction mixture over 2 h. The generator and ice bath were removed, and the reaction stirred under Ar 16 h. The reaction was evaporated, placed briefly under high vacuum, and redissolved in methanol (10 mL). Ammonium carbonate (138 mg, 1.4 mmol) was added. After stirring 19 h, the reaction was evaporated and purified by prep HPLC on a C-18 reverse phase column (20-80% MeCN/H₂O/0.05% TFA) to yield a white powder (84 mg, 48%). ¹H NMR (DMSO-d₆) δ: 10.66 (s, 1H); 9.66 (s, 1H); 9.41 (s, 2H); 8.98 (s, 2H); 8.18 (s, 1H); 8.06 (d, 1H, J=7.6); 7.91 (d, 1H, J=8.5); 7.82 (d, 1H, J=6.9); 7.68 (m, 4H); 7.50 (m, 2H); 7.35 (d, 2H, J=8.8). ¹⁹F NMR (DMSO-d₆) −42.45, −73.86. HRMS calc. for C₂₄H₁₈F₃N₄O₂S, 483.1103; found, 483.1101.

Example 17 3-(3-amidinophenyl)-5-amino-4-[(2′-aminosulfonyl-[1,1]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetic acid salt

Part A. Preparation of methyl N-(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)cyanoacetamide.

Added to the 4-amino-2′-t-butylaminosulfonyl-[1,1′]-biphenyl (2.0 g, 6.6 mmol); in CH₂Cl₂ (10 mL) and stirred at room temp 30 min. A CH₂Cl₂ solution (5 mL) of methyl cyanoacetate (0.58 mL, 6.6 mmol) was added and stirred 1 day. The reaction was quenched carefully with 1 M HCl and extracted into CH₂Cl₂. The organic was extracted again with water and brine, dried over MgSO₄, filtered, and evaporated. The crude mixture was chromatographed on silica gel (50% EtOAc/hexanes) to yield a yellow solid (0.81 g, 33%). ¹H NMR (CDCl₃) δ: 8.74 (s, 1H); 8.16 (d, J=7.7, 1H); 7.64 (d, J=8.8, 2H); 7.58 (d, J=7.3, 1H); 7.66 (d, J=8.1, 1H); 7.46 (d, J=8.4, 2H); 7.31 (d, J=7.7, 1H); 3.89 (s, 1H); 3.63 (s, 2H); 1.04 (s, 9H). MS (NH₃-CI) m/z 389 (M+NH₃).

Part B. Preparation of 3-(3-cyanophenyl)-5-amino-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetate salt.

Methyl N-(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)cyanoacetamide (0.81 g, 2.18 mmol) was added to a solution of triethylmine (0.33 g, 3.27 mmol) in 25 mL of ethanol and 5 mL of CH₂Cl₂. A solution of 3-cyanobenzenehydroximinoyl chloride (0.39 g, 2.18 mmol) in 10 mL ethanol was added slowly over 12 hours via a syringe pump. The reaction mixture was diluted with 50 mL of ether and washed three times with 10 mL of water and twice with 10 mL saturated NaHCO₃, then dried with MgSO₄ and concentrated in vacuo. The resulting off-white solid was purified by prep HPLC on a C-18 reverse phase-column (30-100% MeCN/H₂O/0.05% TFA) to yield a white powder (0.10 g, 8.3%). ¹H NMR (CDCl₃) δ: 9.09 (s, 1H); 8.03 (s, 1H); 7.99 (d, J=6.2, 1H); 7.92 (t, J=7.7, 2H); 7.72 (br s, 2H); 7.59 (t, J=7.7, 1H); 7.53 (m, 2H); 7.45 (d, J=8.4, 2H); 7.26 (d, J=8.4, 2H); 7.25 (m, 1H); 6.51 (s, 1H), 0.97 (s, 9H). MS (NH₃-CI) m/z 273.0 (M+H).

Part C. Preparation of 3-(3-amidinophenyl)-5-amino-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole, trifluoroacetate salt.

3-(3-cyanophenyl)-5-amino-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole (0.10 g, 0.19 mmol) was dissolved in 1 mL of methanol and 4 mL of chloroform. The reaction mixture was cooled in an ice-bath and HCl gas was bubbled-in for 10 minutes to saturate the solution. The mixture was sealed and allowed to stir at room temperature for 14 hours. The solvents were removed in vacuo and the resulting solid was used in the next step.

The imidate formed above was added with 0.07 g (0.95 mmol) of ammonium carbonate and 10 mL of methanol. The mixture was allowed to stir under N₂ for 14 hours. The solvent was removed at reduced pressure. The crude benzamidine was purified by HPLC (C18 reversed phase) eluting with 0.5% TFA in H₂O/CH₃CN to give 0.0064 g (7%) of the desired salt. ¹H NMR (DMSO-d₆)δ: 9.39 (br s, 2H); 9.12 (s, 1H); 8.96 (br s, 2H); 8.06 (s, 1H); 7.98 (d, J=7.7, 1H); 7.96 (d, J=7.8, 1H); 7.88 (d, J=7.7, 1H); 7.74 (br s, 2H); 7.70 (t, J=7.8, 1H); 7.54 (m, 3H); 7.42 (d, J=8.8, 2H); 7.26 (d, J=8.8, 2H); 7.25 (m, 1H); 7.21 (br s, 2H); 6.51 (s, 1H). HRMS m/z 477.1338 (M+H).

Example 18 2-(Phenylamino)-4-(3-amidinopbenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Part A. Preparation of ethyl 3-(3-cyanophenyl)-3-oxopropionate.

To a suspension of sodium hydride (1.2 g of 60% suspension in mineral oil, hexane-washed, 30.3 mmol) in 40 mL of tetrahydrofuran was added diethyl carbonate (3.7 mL, 30.3 mmol) and 3-acetyl benzonitrile (2.2 g, 15.2 mmol). The resulting suspension was stirred at 65° C. for 1 h and then was cooled to room temperature. There was added 40 mL of 10% aqueous HCl and the reaction mixture was diluted with ethyl acetate and the layers were separated. The organic layer was washed with brine, dried (MgSO₄) and concentrated in vacuo to afford 3.2 g (96%) of the title compound, which was sufficiently pure to be used without purification. MS (NH₃-CI) 218.3 (M+H)+.

Part B. Preparation of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate.

According to the procedure of Example 7, Part C, ethyl 3-(3-cyanophenyl)-3-oxopropionate (3.2 g, 14.7 mmol) was converted into the crude bromide, which was purified by flash chromatography (elution with 4:1 hexanes/ethyl acetate) to afford 2.1 g (48%) of the title compound. MS (H₂O, GC/MS) 296/298 (M+H)+.

Part C. Preparation of 2-(phenylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (0.60 g, 2.03 mmol) in 20 mL of absolute ethanol was added N-phenylthiourea (0.31 g, 2.03 mmol). The resulting mixture was stirred at 80° C. for 3 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl ether left the title compound as an off-white solid (0.35 g, 49%). MS. (NH³-CI) 350 (M+H)+.

Part D. Preparation of 2-(phenylamino)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-(phenylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole (0.29 g, 0.83 mmol) was converted into 0.37 g (74%) of the title compound as a solid. MS (ESI) 608.3 (M+H)+.

Part E. Preparation of 2-(phenylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Following the procedure of Example 9, Part C, 2-(phenylamino)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (350 mg, 0.58 mmol) was converted into 50 mg of the title compound (12%) as an off-white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 10.70 (s, 1H), 10.25 (s, 1H), 9.41 (broad s, 2H), 9.02 (broad s, 2H), 8.19 (m, 1H), 8.08 (d, 1H, J=7.7 Hz), 8.03 (d, 1H, J=8.0 Hz), 7.73-7.54 (m, 8H), 7.41-7.27 (m, 8H). MS (ESI) 569.0 (M+H)+.

Example 19 2-(Benzylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)amdnocarbonyl]thiazole, trifluoroacetic acid salt.

Part A. Preparation of 2-(benzylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (0.60 g, 2.03 mmol) in 20 mL of absolute ethanol was added N-benzylthiourea (0.34 g, 2.03 mmol). The resulting mixture was stirred at 80° C. for 3 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl ether left the title compound as an off-white solid (0.36 g, 49%). MS (ESI) 364.1 (M+H)+.

Part B. Preparation of 2-(benzylamino)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-(benzylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole (0.27 g, 0.74 mmol) was converted into 0.30 g (65%) of the title compound as a yellowwash solid. MS (ESI) 622.3 (M+H)+.

Part C. Preparation of 2-(benzylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Following the procedure of Example 9, Part C, 2-(benzylamino)-4-(3-cyanophenyl)-5-[(2′-tertbutylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (260 mg, 0.42 mmol) was converted into 95 mg of the title compound (33%) as an off-white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 9.97 (s, 1H), 9.36 (broad s, 2H), 8.98 (broad s, 2H), 8.78 (t, 1H, J=5.9 Hz), 8.09 (broad s, 1H), 8.02 (dd, 1H, J=7.8, 1.6 Hz), 7.98 (d, 1H, J=7.8 Hz), 7.76 (d, 1H, J=8.0 Hz), 7.66-7.25 (m, 15H), 4.58 (d, 2H, J=5.9 Hz). MS (ESI) 583.0 (M+H)+.

Examples 20 and 21 2-(methylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 20) and 2-(methylamino)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 21)

Part A. Preparation of 2-(methylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (0.65 g, 2.2 mmol) in 20 mL of tetrahydrofuran was added N-methylthiourea (0.20 g, 2.2 mmol). The resulting mixture was stirred at 65° C. for 16 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl ether left the title compound as an off-white solid (0.46 g, 73%). MS (ESI) 288.3 (M+H)+.

Part B. Preparation of 2-(methylamino)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-(methylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole (0.46 g, 1.6 mmol) was converted into 0.68 g (78%) of the title compound as a yellowish solid. MS (ESI) 546.7 (M+H)+.

Part C. Preparation of 2-(methylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 6) and 2-(methylamino)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 20).

Following the procedure of Example 9, Part C, 2-(methylamino)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (500 mg, 1.0 mmol) was converted into 85 mg of the title compound (13%), 2-(methylamino)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 20) as a white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 9.89 (s, 1H), 9.33 (broad s, 2H), 8.96 (broad s, 2H), 8.05 (broad s, 1H), 7.95 (m, 2H), 7.72 (d, 1H, J=8.0 Hz), 7.62-7.44 (m, 6H), 7.29-7.21 (m, 5H), 2.89 (d, 3H). MS (ESI) 507.2 (M+H)+. There was also isolated 50 mg (8%) of 2-(methylamino)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 21). MS (ESI) 508.1 (M+H)+.

Examples 22 and 23 2-methyl-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 22) and 2-methyl-4-(3-carboxamidophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (Example 23)

Part A. Preparation of 2-methyl-4-(3-cyanophenyl)-5-carboxythiazole.

To a solution of of 2-methyl-4-(3-cyanophenyl)-5-carbomethoxythiazole from Example 9, Part A (0.96 g, 3.7 mmol) in 20 mL of tetrahydrofuran and 10 mL of water was added lithium hydroxide monohydrate (0.31 g, 7.4 mmol). The resulting mixture was stirred at room temperature for 16 h. The mixture was concentrated in vacuo, diluted with H₂O and saturated aqueous NaHCO₃ and extracted with hexane. The organic layer was discarded and the aqueous layer was acidified and extracted twice with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried over MgSO₄ and concentrated in vacuo to afford 0.90 g (99%) of the title compound, which was sufficiently pure to be used without purification. MS (NH3-CI) 245 (M+H)+.

Part B. Preparation of 2-methyl-4-(3-cyanophenyl)-5-[[5-(2′-tert-butylaminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole.

To a solution of 2-methyl-4-(3-cyanophenyl)-5-carboxythiazole (0.22 g, 0.89 mmol) in 10 mL of acetonitrile was added thionyl chloride (0.60 g, 5.0 mmol) and 2 drops of dimethylformamide. The resulting solution was allowed to stir at 50° C. for 10 min and then at room temperature for 1 h. The solution was concentrated in vacuo, the residue was dissolved in 20 mL of methylene chloride and then [[5-(2′-tert-butylaminosulfonylphenyl-1-yl)pyridin-2-yl]amine (0.30 g, 0.98 mmol) and triethylamine (1.3 mL, 8.9 mmol) were added. The reaction mixture was allowed to stir at 25° C. for 16 h. The reaction was diluted with ethyl acetate, washed with 10% aq HCl, saturated aq NaHCO₃ and brine, dried (MgSO₄); filtered through a pad of silica gel and concentrated in vacuo. The residue was purified by flash chromatography (elution with 3:1 hexanes/ethyl acetate) to afford 0.07 g (15%) of the title compound. MS (ESI) 532.2 (M+H)+.

Part C. Preparation of 2-methyl-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 22) and 2-methyl-4-(3-carboxamidophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (Example 23).

Following the procedure described in Example 9, Part C, 2-methyl-4-(3-cyanophenyl)-5-[[5-(2′-tert-butylaminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (0.07 g, 0.14 mmol) was converted into 10 mg (16%) of 2-methyl-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl)thiazole, trifluoroacetic acid salt (Example 22) following HPLC purification. MS (ESI) 493.1 (M+H)+. There was also isolated 25 mg (29%) of 2-methyl-4-(3-carboxamidophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (Example 23). MS (ESI) 494.1 (M+H)+.

Examples 24 and 25 2-(3-pyridyl)-4-(3-anidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)anainocarbonyl]thiazole, trifluoroacetic acid salt (Example 24) and 2-(3-pyridyl)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 25)

Part A. Preparation of 2-(3-pyridyl)-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (1.0 g, 3.4 mmol) in 20 mL of tetrahydrofuran was added thionicotinamide (0.46 g, 3.4 mmol). The resulting mixture was stirred at 65° C. for 16 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was triturated with chloroform, taken up in ethyl acetate, washed with saturated aq Na₂CO₃ and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with ethyl acetate left the title compound as an off-white solid (0.26 g, 23%). MS (ESI) 336.1 (M+H)+.

Part B. Preparation of 2-(3-pyridyl)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

4-(3-cyanophenyl)-5-carboethoxythiazole (0.26 g, 0.77 mmol) was converted into 0.24 g (52%) of the title compound as a yellowish solid. MS (ESI) 594.1 (M+H)+.

Part C. Preparation of 2-(3-pyridyl)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 24) and 2-(3-pyridyl)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 25).

Following the procedure of Example 9, Part C, 2-(3-pyridyl)-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (0.24 g, 0.45 mmol) was converted into 80 mg of the title compound (27%) of 2-(3-pyridyl)-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 24) as a white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 10.82 (s, 1H), 9.41 (broad s, 2H), 9.30 (broad s, 1H), 9.02 (broad s, 2H), 8.75 (d, 1H, J=5.5 Hz), 8.43 (d, 1H, J=8 Hz), 8.30 (broad s, 1H), 8.10 (d, 1H, J=8 Hz), 7.98 (d, 1H, J=8 Hz), 7.82 (d, 1H, J=8 Hz), 7.70 (t, 1H, J=8 Hz), 7.62-7.50 (m, 5H), 7.38-7.22 (m, 5H). MS (ESI) 555.0 (M+H)+. There was also isolated 30 mg (10%) of 2-(3-pyridyl)-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 25). ¹H NMR (DMSO-d₆) δ: 10.72 (s, 1H), 9.28 (broad s, 1H), 8.75 (broad s, 1H), 8.42 (m, 2H), 8.09 (broad s, 1H), 7.98 (d, 1H, J=8 Hz), 7.90 (m, 2H), 7.62-7.50 (m, 6H), 7.42 (broad s, 1H), 7.37-7.26 (m, 3H), 7.21 (broad s, 2H). MS (ESI) 578.0 (M+Na)+.

Examples 26 and 27 2-chloro-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)arinocarbonyl]thiazole, trifluoroacetic acid salt (Example 26) and 2-chloro-4-(3-carboxamidophenyl)-5-t(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 27)

Part A. Preparation of 2-amino-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (4.0 g, 13.5 mmol) in 100 mL of tetrahydrofuran was added thiourea (1.03 g, 13.5 mmol). The resulting mixture was stirred at 65° C. for 16 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was triturated with ether, taken up in ethyl acetate, washed with saturated aq Na2CO3 and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with ethyl ether left the title compound as an off-white solid (3.79 g, 98%).

Part B. Preparation of 2-chloro-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a suspension of anhydrous copper (II) chloride (1.86 g, 13.9 mmol) in 180 mL of acetonitrile was added tert-butyl nitrite (1.43 g, 1.39 mmol). The solution was warmed to reflux and then 2-amino-4-(3-cyanophenyl)-5-carboethoxythiazole (3.79 g, 13.9 mmol) in 50 mL of acetonitrile was added via addition funnel over 5 min. The mixture was stirred at reflux until gas evoultion ceased (about 30 min). The reaction was cooled to room temperature, poured into 10% aq Hcl and extracted with ether. The ether layer was washed with saturated aq NaHCO3 and brine, dried (MgSO₄) and concentrated to afford 3.44 g (82%) of the title compound which was used without purification. MS (NH3-CI) 293.2 (M+H)+.

Part C. Preparation of 2-chloro-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Cyanophenyl)-5-carboethoxythiazole (0.084 g, 0.3 mmol) was converted into 0.056 g (34%) of the title compound as a solid. MS (ESI) 551.0 (M+H)+.

Part D. Preparation of 2-chloro-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 26) and 2-chloro-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 27).

Following the procedure of Example 9, Part C, 2-chloro-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (0.056 g, 0.11 mmol) was converted into 15 mg of the title compound (23%) of 2-chloro-4-(3-amidinophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 26) as a white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 10.77 (s, 1H), 9.40 (broad s, 2H), 8.96 (broad s, 2H), 8.15 (broad s, 1H), 7.98 (m, 2H), 7.80 (d, 1H, J=8 Hz), 7.69 (d, 1H, J=8 Hz), 7.61-7.52 (m, 4H), 7.37-7.23 (m, 5H). MS (ESI) 512.0 (M+H)+. There was also isolated 20 mg (31%) of 2-chloro-4-(3-carboxamidophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (Example 27). ¹H NMR (DMSO-d₆) δ: 10.68 (s, 1H), 8.28 (broad s, 1H), 8.05 (broad s, 1H), 7.98 (d, 1H, J=8 Hz), 7.89 (d, 1H, J=8 Hz), 7.78 (d, 1H, J=8 Hz), 7.61-7.52 (m, 5H), 7.40 (broad s, 1H), 7.37-7.23 (m, 3H), 7.21 (broad s, 2H). MS (ESI) 534.9 (M+Na)+.

Examples 28, 29 and 30 2-chloro-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 28), 2-chloro-4-(3-carboxamidophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (Example 29), and 2-hydroxy-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 30)

Part A. Preparation of 2-chloro-4-(3-cyanophenyl)-5-carboxythiazole.

To a solution of of 2-chloro-4-(3-cyanophenyl)-5-carboethoxythiazole (0.44 g, 1.45 mmol) in 25 mL of methanol and 25 mL of water was added potassium hydroxide (0.09 g, 1.6 mmol). The resulting solution was stirred at reflux for 2 h and then was cooled to room temperature. The methanol was removed in vacuo and the aqueous layer was diluted with water and washed with hexanes. The hexane layer was discarded. The aqueous layer was acidified and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried (MgSO₄) and concentrated to yield 0.33 g (97%) of the title compound which was used without further purification. MS (ESI)−262.9 (M−H)−.

Part B. Preparation of 2-chloro-4-(3-cyanophenyl)-5-[[5-(2′-tert-butylaminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole.

Following the procedure described in Example 22, Part B, 2-chloro-4-(3-cyanophenyl)-5-carboxythiazole (0.35 g, 1.33 mmol) was converted into 0.20 g (27%) of the title compound. MS (ESI) 552.0 (M+H)+.

Part C. Preparation of 2-chloro-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 28) and 2-chloro-4-(3-carboxamidophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 29) and 2-hydroxy-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 30).

Following the procedure described in Example 3, Part C, 2-chloro-4-(3-cyanophenyl)-5-[[5-(2′-tert-butylaminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (0.20 g, 0.4 mmol) was converted into 75 mg (32%) of 2-chloro-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 28) following HPLC purification. ¹H NMR (DMSO-d₆) δ: 9.38 (broad s, 2H), 8.98 (broad s, 2H), 8.28 (d, 1H, J=1.5 Hz), 8.15 (broad s, 1H), 8.03-7.96 (m, 3H), 7.81 (m, 2H), 7.70-7.57 (m, 4H), 7.40 (broad s, 1H), 7.36 (m,2H). MS (ESI) 513.0 (M+H)+. There was also isolated 2-chloro-4-(3-carboxamidophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole (Example 29). MS (ESI) 513.9 (M+H)+. There was also isolated 2-hydroxy-4-(3-amidinophenyl)-5-[[5-(2′-aminosulfonylphenyl-1-yl)pyridin-2-yl]aminocarbonyl]thiazole, trifluoroacetic acid salt (Example 30). MS (ESI) 495.0 (M+H)+.

Example 31 2-Chloro-4-(3-aminophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of ethyl 3-(3-nitrophenyl)-3-oxopropionate.

To a suspension of anhydrous tin (II) chloride (2.5 g, 13.2 mmol) in 150 mL of methylene chloride was added ethyl diazoacetate (8.3 g, 72.8 mmol). Then 3-nitrobenzaldehyde (10.0 g, 66.2 mmol) was added as a solid in small portions over 30 min. The resulting suspension was stirred at room temperature for 24 h. Additional tin (II) chloride (2.5 g) was added and the reaction was stirred an additional 24 h. The reaction was concentrated in vacuo, diluted with ethyl acetate, washed with water (2 times) and brine, dried (MgSO₄) and concentrated. The residue was purified by flash chromatography (elution with 4:1 hexanes/ethyl acetate) to afford 5 g (32%) of the title compound. ¹H NMR (CDCl₃) (approximately 12:1 mixture of enol and keto tautomers, data for enol only) δ: 12.6 (s, 1H); 8.60 (t, 1H, J=1.8 Hz); 8.3 (m, 1H); 8.1 (m, 1H); 7.62 (t, 1H, J=7.9 Hz) 5.77 (s, 1H); 4.30 (q, 2H, J=7.2 Hz); 1.35 (t, 3H, J=7.2 Hz).

Part B. Preparation of 2-amino-4-(3-nitrophenyl)-5-carboethoxythiazole.

To a solution of ethyl 3-(3-nitrophenyl)-3-oxopropionate (3.45 g, 14.5 mmol) in 100 mL of acetonitrile was added hydroxy(tosyloxy)iodobenzene (6.3 g, 16.0 mmol). The resulting suspension was stirred at 65° C. for 1 h at which time the reaction was a homogeneous solution. Thiourea (1.22 g, 16.0 mmol) was added and stirring was continued at 65° C. for 2 h. The mixture was cooled and concentrated, and the residue was taken up in ethyl acetate, washed with saturated aq Na2CO3 and brine, dried (MgSO₄) and concentrated. The residue was triturated with ethyl ether to afford 3.0 g (71%) of the title compound as a yellow solid. ¹H NMR (DMSO-d₆) δ: 8.47 (t, 1H, J=1.9 Hz); 8.24 (m, 1H); 8.21 (m, 1H); 7.97 (broad s, 2H); 7.65 (t, 1H, J=8.1 Hz); 4.08 (q, 2H, J=7.1 Hz); 1.11 (t, 3H, J=7.1 Hz).

Part C. Preparation of 2-amino-4-(3-nitrophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-amino-4-(3-nitrophenyl)-5-carboethoxythiazole (0.30 g, 1.02 mmol) was converted into 0.22 g (39%) of the title compound as a solid. MS (ESI) 574.0 (M+Na)+.

Part D. Preparation of 2-chloro-4-(3-nitrophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure described in Example 26, Part B, 2-amino-4-(3-nitrophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (155 mg, 0.28 mmol) was converted into 150 mg (94%) of the title compound which was used without purification. MS (NH₃-CI) 588 (M+NH4)+.

Part E. Preparation of 2-chloro-4-(3-aminophenyl)-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

To a solution of 2-chloro-4-(3-nitrophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (100 mg, 0.18 mmol) in ethyl acetate was added tin (II) chloride dihydrate (0.32 g, 1.4 mmol). The resulting suspension was stirred at reflux for 2 h and then was cooled and quenched with saturated aq NaHCO₃. The reaction was diluted with ethyl acetate, washed with brine, dried (MgSO₄) and concentrated to yield 90 mg (93%) of an amine which was used without purification. The residue was taken up in 5 mL of trifluoroacetic acid and stirred at reflux for 15 min. The reaction was concentrated and the residue was purified by prep HPLC to afford 40 mg (37%) of the title compound as a white powder. ¹H NMR (DMSO-d₆) δ: 10.67 (s, 1H), 7.98 (d, 1H, J=8 Hz), 7.60-7.50 (m, 4H), 7.34-7.19 (m, 7H), 7.11 (broad m, 1H), 6.84 (broad m, 1H). MS (ESI) 484.9 (M+H)+.

Example 32 2-amino-4-[(3-amino-4-chloro)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of ethyl 3-[(3-nitro-4-chloro)phenyl]-3-oxopropionate.

Following the procedure described in Example 31, Part A, 4-chloro-3-nitrobenzaldehyde (10.0 g, 53.9 mmol) was converted into 4.8 g (33%) of the title compound as a yellow solid. ¹H NMR (CDCl₃) (approximately 15:1 mixture of enol and keto tautomers, data for enol only) δ: 12.6 (s, 1H); 8.25 (d, 1H); 7.9 (dd, 1H); 7.6 (d, 1H) 5.7 (s, 1H); 4.27 (q, 2H); 1.35 (t, 3H).

Part B. Preparation of 2-amino-4-[(3-nitro-4-chloro)phenyl]-5-carboethoxythiazole.

Following the procedure described in Example 31, Part B, ethyl 3-[(3-nitro-4-chloro)phenyl]-3-oxopropionate (1.6 g, 5.9 mmol) was converted into the title compound as a yellow solid. ¹H NMR (DMSO-d₆) δ: 8.32 (d, 1H); 7.98 (s, 2H); 7.95 (d, 1H); 7.75 (d, 1H); 4.08 (q, 2H); 1.13 (t, 3H).

Part C. Preparation of 2-amino-4-[(3-nitro-4-chloro)phenyl]-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-amino-4-[(3-nitro-4-chloro)phenyl]-5-carboethoxythiazole (0.49 g, 1.5 mmol) was converted into 0.79 g (89%) of the title compound as a solid. MS (ESI) 586.0 (M+H)+.

Part D. Preparation of 2-amino-4-[(3-amino-4-chloro)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Following the procedure described in Example 31, Part E, 2-amino-4-[(3-nitro-4-chloro)phenyl]-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (100 mg, 0.17 mmol) was converted into 35 mg (41%) of the title compound which was a white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 9.68 (s, 1H), 7.98 (d, 1H, J=8 Hz), 7.60-7.43 (m, 5H), 7.30-7.10 (m, 8H), 6.75 (dd, 1H, J=8, 2 Hz). MS (ESI) 499.9 (M+H)+.

Example 33 2-chloro-4-[(3-amino-4-chloro)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of 2-chloro-4-[(3-nitro-4-chloro)phenyl]-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure described in Example 26, Part B, 2-amino-4-[(3-nitro-4-chloro)phenyl]-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (199 mg, 0.34 mmol) was converted into 150 mg (71%) of the title compound. MS (ESI) 626.9 (M+Na)+.

Part B. Preparation of 2-chloro-4-[(3-amino-4-chloro)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

Following the procedure described in Example 31, Part E, 2-chloro-4-[(3-nitro-4-chloro)phenyl]-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (107 mg, 0.18 mmol) was converted into 10 mg (11%) of the title compound which was a white powder following HPLC purification. ¹H NMR (DMSO-d₆) δ: 10.66 (s, 1H), 7.99 (d, 1H, J=8.0 Hz), 7.60-7.50 (m, 4H), 7.37-7.20 (m, 7H), 6.81 (dd, 1H, J=8.0, 2 Hz). MS (ESI) 518.9 (M+H)+.

Example 34 2-amino-4-[(3-aminomethyl)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt

Part A. Preparation of 2-amino-4-(3-cyanophenyl)-5-carboethoxythiazole.

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (2.0 g, 6.75 mmol) in 100 mL of absolute ethanol was added thiourea (0.51 g, 6.75 mmol). The resulting mixture was stirred at 80° C. for 3 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with saturated aq NaHCO₃ and brine, dried (MgSO₄) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl ether left the title compound as an off-white solid (1.55 g, 65%). ¹H NMR (DMSO-d₆) δ: 8.03 (s, 1H); 7.93 (s, 2H); 7.91 (d, 1H); 7.82 (d, 1H); 7.58 (t, 1H); 4.05 (q, 2H); 1.10 (t, 3H).

Part B. Preparation of 2-amino-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole.

Following the procedure of Example 7, Part E, 2-amino-4-(3-cyanophenyl)-5-carboethoxythiazole (0.49 g, 1.8 mmol) was converted into 0.31 g (32%) of the title compound as a solid. MS (ESI) 532.3 (M+H)+.

Part C. Preparation of 2-amino-4-[(3-aminomethyl)phenyl]-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole, trifluoroacetic acid salt.

To a solution of lithium aluminum hydride (0.63 mL of a 1.0 M solution in tetrahydrofuran, 0.63 mmol) in 10 mL of tetrahydrofuran at 0° C. was added concentrated H₂SO₄ (0.020 mL, 0.32 mmol). This solution was stirred for 30 min and then 2-amino-4-(3-cyanophenyl)-5-[(2′-tert-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]thiazole (112 mg, 0.21 mmol) was added as a solution in tetrahydrofuran. The resulting mixture was allowed to warm to room temperature and then was stirred for 16 h. The reaction was cooled to 0° C. and quenched by dropwise addition of water. Dilute aqueous NaOH was added and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO₄) and concentrated. The residue was taken up in 5 mL of trifluoroacetic acid and stirred at reflux for 30 min. This mixture was cooled and concentrated in vacuo. The residue was purified by prep HPLC to afford the title compound as a white powder. ¹H NMR (DMSO-d₆) δ: 9.77 (s, 1H), 8.13 (broad s, 3H), 7.97 (d, 1H, J=8 Hz), 7.71 (s, 1H), 7.60-7.40 (m, 8H), 7.29-7.20 (m, 6H), 3.98 (broad q, 2H). MS (ESI) 480.0 (M+H)+.

TABLE 1

Ex. Ring M D R R^(1a) R^(4a) A′ MS  1 isoxazole C(═NH)NH₂ H CH₂OH SO₂NH₂ CH 492.1  2 isoxazole C(═NH)NH₂ H H SO₂NH₂ CH 462.1  3 isoxazole C(═NH)NH₂ H H SO₂Me CH 461.1  4 isoxazole C(═NH)NH₂ H CH₂OMe SO₂NH₂ N 506.1  5 isoxazole C(═NH)NH₂ H H CF₃ CH 451.1  6 isoxazole C(═NH)NH₂ H CF₃ SO₂NH₂ CH 530.1  7 thiazole C(═NH)NH₂ H NHAc SO₂NH₂ CH 535.0  8 thiazole C(═NH)NH₂ H NH₂ SO₂NH₂ CH 493.0  9 thiazole C(═NH)NH₂ H CH₃ SO₂NH₂ CH 492.3 10 oxazole C(═NH)NH₂ H H SO₂NH₂ CH 462.1 11 isoxazole C(═NH)NH₂ H H SO₂NHtBu CH 518.2 12 isoxazole C(═NH)NH₂ H CH₂OMe SO₂NH₂ CH 506.1 13 thiazole C(═NH)NH₂ H Me CF₃ CH 481.3 14 thiazole C(═NH)NH₂ H Ph SO₂NH₂ CH 554.3 15 isoxazole C(═NH)NH₂ H H SO₂Me CF 479.1 16 isoxazole C(═NH)NH₂ H H SCF₃ CH 483.1 17 isoxazole C(═NH)NH₂ H NH₂ SO₂NH₂ CH 477.1 18 thiazole C(═NH)NH₂ H NHPh SO₂NH₂ CH 569.0 19 thiazole C(═NH)NH₂ H NHCH₂Ph SO₂NH₂ CH 583.0 20 thiazole C(═NH)NH₂ H NHMe SO₂NH₂ CH 507.2 21 thiazole CONH₂ H NHMe SO₂NH₂ CH 508.1 22 thiazole C(═NH)NH₂ H Me SO₂NH₂ N 493.1 23 thiazole CONH₂ H Me SO₂NH₂ N 494.1 24 thiazole C(═NH)NH₂ H 3-pyridyl SO₂NH₂ CH 554.3 25 thiazole CONH₂ H 3-pyridyl SO₂NH₂ CH 578.0 (M + Na)⁺ 26 thiazole C(═NH)NH₂ H Cl SO₂NH₂ CH 512.0 27 thiazole CONH₂ H Cl SO₂NH₂ CH 534.9 (M + Na)⁺ 28 thiazole C(═NH)NH₂ H Cl SO₂NH₂ N 513.0 29 thiazole CONH₂ H Cl SO₂NH₂ N 513.9 30 thiazole C(═NH)NH₂ H OH SO₂NH₂ N 495.0 31 thiazole NH₂ H Cl SO₂NH₂ CH 484.9 32 thiazole NH₂ Cl NH₂ SO₂NH₂ CH 499.9 33 thiazole NH₂ Cl Cl SO₂NH₂ CH 518.9 34 thiazole CH₂NH₂ H NH₂ SO₂NH₂ CH 480.0

The following tables contain representative examples of the present invention. Each entry in each table is intended to be paired with each formulae at the start of the table. For example, example 1 in Table 2 is intended to be paired with each of formulae A-BB and example 1 in Table 3 is intended to be paired with each of fomulae a-dd.

The following groups are intended for group A in the tables.

TABLE 2

Ex # R^(1a) A B 1 CH₃ phenyl 2-(aminosulfonyl)phenyl 2 CH₃ phenyl 2-(methylaminosulfonyl)phenyl 3 CH₃ phenyl 1-pyrrolidinocarbonyl 4 CH₃ phenyl 2-(methylsulfonyl)phenyl 5 CH₃ phenyl 4-morpholino 6 CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 7 CH₃ phenyl 4-morpholinocarbonyl 8 CH₃ phenyl 2-methyl-1-imidazolyl 9 CH₃ phenyl 5-methyl-1-imidazolyl 10 CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 11 CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 12 CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 13 CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 14 CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 15 CH₃ 2-pyridyl 4-morpholino 16 CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 17 CH₃ 2-pyridyl 4-morpholinocarbonyl 18 CH₃ 2-pyridyl 2-methyl-1-imidazolyl 19 CH₃ 2-pyridyl 5-methyl-1-imidazolyl 20 CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 21 CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 22 CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 23 CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 24 CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 25 CH₃ 3-pyridyl 4-morpholino 26 CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 27 CH₃ 3-pyridyl 4-morpholinocarbonyl 28 CH₃ 3-pyridyl 2-methyl-1-imidazolyl 29 CH₃ 3-pyridyl 5-methyl-1-imidazolyl 30 CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 31 CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 32 CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 33 CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 34 CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 35 CH₃ 2-pyrimidyl 4-morpholino 36 CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 37 CH₃ 2-pyrimidyl 4-morpholinocarbonyl 38 CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 39 CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 40 CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 41 CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 42 CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 43 CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 44 CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 45 CH₃ 5-pyrimidyl 4-morpholino 46 CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 47 CH₃ 5-pyrimidyl 4-morpholinocarbonyl 48 CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 49 CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 50 CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 51 CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 52 CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 53 CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 54 CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 55 CH₃ 2-Cl-phenyl 4-morpholino 56 CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 57 CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 58 CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 59 CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 60 CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 61 CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 62 CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 63 CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 64 CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 65 CH₃ 2-F-phenyl 4-morpholino 66 CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 67 CH₃ 2-F-phenyl 4-morpholinocarbonyl 68 CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 69 CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 70 CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 71 CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 72 CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 73 CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 74 CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 75 CH₃ 2,6-diF-phenyl 4-morpholino 76 CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 77 CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 78 CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 79 CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 80 CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 81 CH₂CH₃ phenyl 2-(aminosulfonyl)phenyl 82 CH₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 83 CH₂CH₃ phenyl 1-pyrrolidinocarbonyl 84 CH₂CH₃ phenyl 2-(methylsulfonyl)phenyl 85 CH₂CH₃ phenyl 4-morpholino 86 CH₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 87 CH₂CH₃ phenyl 4-morpholinocarbonyl 88 CH₂CH₃ phenyl 2-methyl-1-imidazolyl 89 CH₂CH₃ phenyl 5-methyl-1-imidazolyl 90 CH₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 91 CH₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 92 CH₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 93 CH₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 94 CH₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 95 CH₂CH₃ 2-pyridyl 4-morpholino 96 CH₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 97 CH₂CH₃ 2-pyridyl 4-morpholinocarbonyl 98 CH₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 99 CH₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 100 CH₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 101 CH₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 102 CH₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 103 CH₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 104 CH₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 105 CH₂CH₃ 3-pyridyl 4-morpholino 106 CH₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 107 CH₂CH₃ 3-pyridyl 4-morpholinocarbonyl 108 CH₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 109 CH₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 110 CH₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 111 CH₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 112 CH₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 113 CH₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 114 CH₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 115 CH₂CH₃ 2-pyrimidyl 4-morpholino 116 CH₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 117 CH₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 118 CH₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 119 CH₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 120 CH₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 121 CH₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 122 CH₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 123 CH₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 124 CH₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 125 CH₂CH₃ 5-pyrimidyl 4-morpholino 126 CH₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 127 CH₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 128 CH₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 129 CH₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 130 CH₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 131 CH₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 132 CH₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 133 CH₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 134 CH₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 135 CH₂CH₃ 2-Cl-phenyl 4-morpholino 136 CH₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 137 CH₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 138 CH₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 139 CH₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 140 CH₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 141 CH₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 142 CH₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 143 CH₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 144 CH₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 145 CH₂CH₃ 2-F-phenyl 4-morpholino 146 CH₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 147 CH₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 148 CH₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 149 CH₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 150 CH₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 151 CH₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 152 CH₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 153 CH₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 154 CH₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 155 CH₂CH₃ 2,6-diF-phenyl 4-morpholino 156 CH₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 157 CH₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 158 CH₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 159 CH₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 160 CH₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 161 CF₃ phenyl 2-(aminosulfonyl)phenyl 162 CF₃ phenyl 2-(methylaminosulfonyl)phenyl 163 CF₃ phenyl 1-pyrrolidinocarbonyl 164 CF₃ phenyl 2-(methylsulfonyl)phenyl 165 CF₃ phenyl 4-morpholino 166 CF₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 167 CF₃ phenyl 4-morpholinocarbonyl 168 CF₃ phenyl 2-methyl-1-imidazolyl 169 CF₃ phenyl 5-methyl-1-imidazolyl 170 CF₃ phenyl 2-methylsulfonyl-1-imidazolyl 171 CF₃ 2-pyridyl 2-(aminosulfonyl)phenyl 172 CF₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 173 CF₃ 2-pyridyl 1-pyrrolidinocarbonyl 174 CF₃ 2-pyridyl 2-(methylsulfonyl)phenyl 175 CF₃ 2-pyridyl 4-morpholino 176 CF₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 177 CF₃ 2-pyridyl 4-morpholinocarbonyl 178 CF₃ 2-pyridyl 2-methyl-1-imidazolyl 179 CF₃ 2-pyridyl 5-methyl-1-imidazolyl 180 CF₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 181 CF₃ 3-pyridyl 2-(aminosulfonyl)phenyl 182 CF₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 183 CF₃ 3-pyridyl 1-pyrrolidinocarbonyl 184 CF₃ 3-pyridyl 2-(methylsulfonyl)phenyl 185 CF₃ 3-pyridyl 4-morpholino 186 CF₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 187 CF₃ 3-pyridyl 4-morpholinocarbonyl 188 CF₃ 3-pyridyl 2-methyl-1-imidazolyl 189 CF₃ 3-pyridyl 5-methyl-1-imidazolyl 190 CF₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 191 CF₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 192 CF₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 193 CF₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 194 CF₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 195 CF₃ 2-pyrimidyl 4-morpholino 196 CF₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 197 CF₃ 2-pyrimidyl 4-morpholinocarbonyl 198 CF₃ 2-pyrimidyl 2-methyl-1-imidazolyl 199 CF₃ 2-pyrimidyl 5-methyl-1-imidazolyl 200 CF₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 201 CF₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 202 CF₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 203 CF₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 204 CF₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 205 CF₃ 5-pyrimidyl 4-morpholino 206 CF₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 207 CF₃ 5-pyrimidyl 4-morpholinocarbonyl 208 CF₃ 5-pyrimidyl 2-methyl-1-imidazolyl 209 CF₃ 5-pyrimidyl 5-methyl-1-imidazolyl 210 CF₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 211 CF₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 212 CF₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 213 CF₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 214 CF₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 215 CF₃ 2-Cl-phenyl 4-morpholino 216 CF₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 217 CF₃ 2-Cl-phenyl 4-morpholinocarbonyl 218 CF₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 219 CF₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 220 CF₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 221 CF₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 222 CF₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 223 CF₃ 2-F-phenyl 1-pyrrolidinocarbonyl 224 CF₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 225 CF₃ 2-F-phenyl 4-morpholino 226 CF₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 227 CF₃ 2-F-phenyl 4-morpholinocarbonyl 228 CF₃ 2-F-phenyl 2-methyl-1-imidazolyl 229 CF₃ 2-F-phenyl 5-methyl-1-imidazolyl 230 CF₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 231 CF₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 232 CF₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 233 CF₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 234 CF₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 235 CF₃ 2,6-diF-phenyl 4-morpholino 236 CF₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 237 CF₃ 2,6-diF-phenyl 4-morpholinocarbonyl 238 CF₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 239 CF₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 240 CF₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 241 SCH₃ phenyl 2-(aminosulfonyl)phenyl 242 SCH₃ phenyl 2-(methylaminosulfonyl)phenyl 243 SCH₃ phenyl 1-pyrrolidinocarbonyl 244 SCH₃ phenyl 2-(methylsulfonyl)phenyl 245 SCH₃ phenyl 4-morpholino 246 SCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 247 SCH₃ phenyl 4-morpholinocarbonyl 248 SCH₃ phenyl 2-methyl-1-imidazolyl 249 SCH₃ phenyl 5-methyl-1-imidazolyl 250 SCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 251 SCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 252 SCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 253 SCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 254 SCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 255 SCH₃ 2-pyridyl 4-morpholino 256 SCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 257 SCH₃ 2-pyridyl 4-morpholinocarbonyl 258 SCH₃ 2-pyridyl 2-methyl-1-imidazolyl 259 SCH₃ 2-pyridyl 5-methyl-1-imidazolyl 260 SCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 261 SCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 262 SCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 263 SCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 264 SCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 265 SCH₃ 3-pyridyl 4-morpholino 266 SCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 267 SCH₃ 3-pyridyl 4-morpholinocarbonyl 268 SCH₃ 3-pyridyl 2-methyl-1-imidazolyl 269 SCH₃ 3-pyridyl 5-methyl-1-imidazolyl 270 SCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 271 SCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 272 SCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 273 SCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 274 SCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 275 SCH₃ 2-pyrimidyl 4-morpholino 276 SCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 277 SCH₃ 2-pyrimidyl 4-morpholinocarbonyl 278 SCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 279 SCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 280 SCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 281 SCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 282 SCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 283 SCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 284 SCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 285 SCH₃ 5-pyrimidyl 4-morpholino 286 SCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 287 SCH₃ 5-pyrimidyl 4-morpholinocarbonyl 288 SCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 289 SCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 290 SCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 291 SCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 292 SCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 293 SCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 294 SCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 295 SCH₃ 2-Cl-phenyl 4-morpholino 296 SCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 297 SCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 298 SCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 299 SCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 300 SCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 301 SCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 302 SCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 303 SCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 304 SCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 305 SCH₃ 2-F-phenyl 4-morpholino 306 SCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 307 SCH₃ 2-F-phenyl 4-morpholinocarbonyl 308 SCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 309 SCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 310 SCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 311 SCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 312 SCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 313 SCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 314 SCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 315 SCH₃ 2,6-diF-phenyl 4-morpholino 316 SCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 317 SCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 318 SCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 319 SCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 320 SCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 321 SOCH₃ phenyl 2-(aminosulfonyl)phenyl 322 SOCH₃ phenyl 2-(methylaminosulfonyl)phenyl 323 SOCH₃ phenyl 1-pyrrolidinocarbonyl 324 SOCH₃ phenyl 2-(methylsulfonyl)phenyl 325 SOCH₃ phenyl 4-morpholino 326 SOCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 327 SOCH₃ phenyl 4-morpholinocarbonyl 328 SOCH₃ phenyl 2-methyl-1-imidazolyl 329 SOCH₃ phenyl 5-methyl-1-imidazolyl 330 SOCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 331 SOCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 332 SOCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 333 SOCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 334 SOCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 335 SOCH₃ 2-pyridyl 4-morpholino 336 SOCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 337 SOCH₃ 2-pyridyl 4-morpholinocarbonyl 338 SOCH₃ 2-pyridyl 2-methyl-1-imidazolyl 339 SOCH₃ 2-pyridyl 5-methyl-1-imidazolyl 340 SOCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 341 SOCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 342 SOCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 343 SOCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 344 SOCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 345 SOCH₃ 3-pyridyl 4-morpholino 346 SOCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 347 SOCH₃ 3-pyridyl 4-morpholinocarbonyl 348 SOCH₃ 3-pyridyl 2-methyl-1-imidazolyl 349 SOCH₃ 3-pyridyl 5-methyl-1-imidazolyl 350 SOCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 351 SOCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 352 SOCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 353 SOCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 354 SOCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 355 SOCH₃ 2-pyrimidyl 4-morpholino 356 SOCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 357 SOCH₃ 2-pyrimidyl 4-morpholinocarbonyl 358 SOCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 359 SOCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 360 SOCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 361 SOCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 362 SOCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 363 SOCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 364 SOCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 365 SOCH₃ 5-pyrimidyl 4-morpholino 366 SOCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 367 SOCH₃ 5-pyrimidyl 4-morpholinocarbonyl 368 SOCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 369 SOCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 370 SOCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 371 SOCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 372 SOCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 373 SOCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 374 SOCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 375 SOCH₃ 2-Cl-phenyl 4-morpholino 376 SOCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 377 SOCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 378 SOCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 379 SOCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 380 SOCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 381 SOCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 382 SOCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 383 SOCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 384 SOCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 385 SOCH₃ 2-F-phenyl 4-morpholino 386 SOCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 387 SOCH₃ 2-F-phenyl 4-morpholinocarbonyl 388 SOCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 389 SOCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 390 SOCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 391 SOCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 392 SOCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 393 SOCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 394 SOCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 395 SOCH₃ 2,6-diF-phenyl 4-morpholino 396 SOCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 397 SOCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 398 SOCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 399 SOCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 400 SOCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 401 SO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 402 SO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 403 SO₂CH₃ phenyl 1-pyrrolidinocarbonyl 404 SO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 405 SO₂CH₃ phenyl 4-morpholino 406 SO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 407 SO₂CH₃ phenyl 4-morpholinocarbonyl 408 SO₂CH₃ phenyl 2-methyl-1-imidazolyl 409 SO₂CH₃ phenyl 5-methyl-1-imidazolyl 410 SO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 411 SO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 412 SO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 413 SO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 414 SO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 415 SO₂CH₃ 2-pyridyl 4-morpholino 416 SO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 417 SO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 418 SO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 419 SO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 420 SO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 421 SO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 422 SO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 423 SO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 424 SO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 425 SO₂CH₃ 3-pyridyl 4-morpholino 426 SO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 427 SO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 428 SO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 429 SO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 430 SO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 431 SO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 432 SO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 433 SO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 434 SO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 435 SO₂CH₃ 2-pyrimidyl 4-morpholino 436 SO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 437 SO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 438 SO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 439 SO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 440 SO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 441 SO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 442 SO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 443 SO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 444 SO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 445 SO₂CH₃ 5-pyrimidyl 4-morpholino 446 SO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 447 SO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 448 SO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 449 SO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 450 SO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 451 SO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 452 SO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 453 SO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 454 SO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 455 SO₂CH₃ 2-Cl-phenyl 4-morpholino 456 SO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 457 SO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 458 SO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 459 SO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 460 SO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 461 SO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 462 SO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 463 SO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 464 SO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 465 SO₂CH₃ 2-F-phenyl 4-morpholino 466 SO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 467 SO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 468 SO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 469 SO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 470 SO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 471 SO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 472 SO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 473 SO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 474 SO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 475 SO₂CH₃ 2,6-diF-phenyl 4-morpholino 476 SO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 477 SO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 478 SO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 479 SO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 480 SO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 481 CH₂NH— phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 482 CH₂NH— phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 483 CH₂NH— phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 484 CH₂NH— phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 485 CH₂NH— phenyl 4-morpholino SO₂CH₃ 486 CH₂NH— phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 487 CH₂NH— phenyl 4-morpholinocarbonyl SO₂CH₃ 488 CH₂NH— phenyl 2-methyl-1-imidazolyl SO₂CH₃ 489 CH₂NH— phenyl 5-methyl-1-imidazolyl SO₂CH₃ 490 CH₂NH— phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 491 CH₂NH— 2-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 492 CH₂NH— 2-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 493 CH₂NH— 2-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 494 CH₂NH— 2-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 495 CH₂NH— 2-pyridyl 4-morpholino SO₂CH₃ 496 CH₂NH— 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 497 CH₂NH— 2-pyridyl 4-morpholinocarbonyl SO₂CH₃ 498 CH₂NH— 2-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 499 CH₂NH— 2-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 500 CH₂NH— 2-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 501 CH₂NH— 3-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 502 CH₂NH— 3-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 503 CH₂NH— 3-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 504 CH₂NH— 3-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 505 CH₂NH— 3-pyridyl 4-morpholino SO₂CH₃ 506 CH₂NH— 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 507 CH₂NH— 3-pyridyl 4-morpholinocarbonyl SO₂CH₃ 508 CH₂NH— 3-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 509 CH₂NH— 3-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 510 CH₂NH— 3-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 511 CH₂NH— 2-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 512 CH₂NH— 2-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 513 CH₂NH— 2-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 514 CH₂NH— 2-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 515 CH₂NH— 2-pyrimidyl 4-morpholino SO₂CH₃ 516 CH₂NH— 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 517 CH₂NH— 2-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 518 CH₂NH— 2-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 519 CH₂NH— 2-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 520 CH₂NH— 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 521 CH₂NH— 5-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 522 CH₂NH— 5-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 523 CH₂NH— 5-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 524 CH₂NH— 5-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 525 CH₂NH— 5-pyrimidyl 4-morpholino SO₂CH₃ 526 CH₂NH— 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 527 CH₂NH— 5-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 528 CH₂NH— 5-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 529 CH₂NH— 5-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 530 CH₂NH— 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 531 CH₂NH— 2-Cl-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 532 CH₂NH— 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 533 CH₂NH— 2-Cl-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 534 CH₂NH— 2-Cl-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 535 CH₂NH— 2-Cl-phenyl 4-morpholino SO₂CH₃ 536 CH₂NH— 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 537 CH₂NH— 2-Cl-phenyl 4-morpholinocarbonyl SO₂CH₃ 538 CH₂NH— 2-Cl-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 539 CH₂NH— 2-Cl-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 540 CH₂NH— 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 541 CH₂NH— 2-F-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 542 CH₂NH— 2-F-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 543 CH₂NH— 2-F-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 544 CH₂NH— 2-F-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 545 CH₂NH— 2-F-phenyl 4-morpholino SO₂CH₃ 546 CH₂NH— 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 547 CH₂NH— 2-F-phenyl 4-morpholinocarbonyl SO₂CH₃ 548 CH₂NH— 2-F-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 549 CH₂NH— 2-F-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 550 CH₂NH— 2-F-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 551 CH₂NH— 2,6-diF-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 552 CH₂NH— 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl SO_(2CH) ₃ 553 CH₂NH— 2,6-diF-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 554 CH₂NH— 2,6-diF-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 555 CH₂NH— 2,6-diF-phenyl 4-morpholino SO₂CH₃ 556 CH₂NH— 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 557 CH₂NH— 2,6-diF-phenyl 4-morpholinocarbonyl SO₂CH₃ 558 CH₂NH— 2,6-diF-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 559 CH₂NH— 2,6-diF-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 560 CH₂NH— 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 561 Cl phenyl 2-(aminosulfonyl)phenyl 562 Cl phenyl 2-(methylaminosulfonyl)phenyl 563 Cl phenyl 1-pyrrolidinocarbonyl 564 Cl phenyl 2-(methylsulfonyl)phenyl 565 Cl phenyl 4-morpholino 566 Cl phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 567 Cl phenyl 4-morpholinocarbonyl 568 Cl phenyl 2-methyl-1-imidazolyl 569 Cl phenyl 5-methyl-1-imidazolyl 570 Cl phenyl 2-methylsulfonyl-1-imidazolyl 571 Cl 2-pyridyl 2-(aminosulfonyl)phenyl 572 Cl 2-pyridyl 2-(methylaminosulfonyl)phenyl 573 Cl 2-pyridyl 1-pyrrolidinocarbonyl 574 Cl 2-pyridyl 2-(methylsulfonyl)phenyl 575 Cl 2-pyridyl 4-morpholino 576 Cl 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 577 Cl 2-pyridyl 4-morpholinocarbonyl 578 Cl 2-pyridyl 2-methyl-1-imidazolyl 579 Cl 2-pyridyl 5-methyl-1-imidazolyl 580 Cl 2-pyridyl 2-methylsulfonyl-1-imidazolyl 581 Cl 3-pyridyl 2-(aminosulfonyl)phenyl 582 Cl 3-pyridyl 2-(methylaminosulfonyl)phenyl 583 Cl 3-pyridyl 1-pyrrolidinocarbonyl 584 Cl 3-pyridyl 2-(methylsulfonyl)phenyl 585 Cl 3-pyridyl 4-morpholino 586 Cl 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 587 Cl 3-pyridyl 4-morpholinocarbonyl 588 Cl 3-pyridyl 2-methyl-1-imidazolyl 589 Cl 3-pyridyl 5-methyl-1-imidazolyl 590 Cl 3-pyridyl 2-methylsulfonyl-1-imidazolyl 591 Cl 2-pyrimidyl 2-(aminosulfonyl)phenyl 592 Cl 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 593 Cl 2-pyrimidyl 1-pyrrolidinocarbonyl 594 Cl 2-pyrimidyl 2-(methylsulfonyl)phenyl 595 Cl 2-pyrimidyl 4-morpholino 596 Cl 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 597 Cl 2-pyrimidyl 4-morpholinocarbonyl 598 Cl 2-pyrimidyl 2-methyl-1-imidazolyl 599 Cl 2-pyrimidyl 5-methyl-1-imidazolyl 600 Cl 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 601 Cl 5-pyrimidyl 2-(aminosulfonyl)phenyl 602 Cl 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 603 Cl 5-pyrimidyl 1-pyrrolidinocarbonyl 604 Cl 5-pyrimidyl 2-(methylsulfonyl)phenyl 605 Cl 5-pyrimidyl 4-morpholino 606 Cl 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 607 Cl 5-pyrimidyl 4-morpholinocarbonyl 608 Cl 5-pyrimidyl 2-methyl-1-imidazolyl 609 Cl 5-pyrimidyl 5-methyl-1-imidazolyl 610 Cl 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 611 Cl 2-Cl-phenyl 2-(aminosulfonyl)phenyl 612 Cl 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 613 Cl 2-Cl-phenyl 1-pyrrolidinocarbonyl 614 Cl 2-Cl-phenyl 2-(methylsulfonyl)phenyl 615 Cl 2-Cl-phenyl 4-morpholino 616 Cl 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 617 Cl 2-Cl-phenyl 4-morpholinocarbonyl 618 Cl 2-Cl-phenyl 2-methyl-1-imidazolyl 619 Cl 2-Cl-phenyl 5-methyl-1-imidazolyl 620 Cl 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 621 Cl 2-F-phenyl 2-(aminosulfonyl)phenyl 622 Cl 2-F-phenyl 2-(methylaminosulfonyl)phenyl 623 Cl 2-F-phenyl 1-pyrrolidinocarbonyl 624 Cl 2-F-phenyl 2-(methylsulfonyl)phenyl 625 Cl 2-F-phenyl 4-morpholino 626 Cl 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 627 Cl 2-F-phenyl 4-morpholinocarbonyl 628 Cl 2-F-phenyl 2-methyl-1-imidazolyl 629 Cl 2-F-phenyl 5-methyl-1-imidazolyl 630 Cl 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 631 Cl 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 632 Cl 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 633 Cl 2,6-diF-phenyl 1-pyrrolidinocarbonyl 634 Cl 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 635 Cl 2,6-diF-phenyl 4-morpholino 636 Cl 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 637 Cl 2,6-diF-phenyl 4-morpholinocarbonyl 638 Cl 2,6-diF-phenyl 2-methyl-1-imidazolyl 639 Cl 2,6-diF-phenyl 5-methyl-1-imidazolyl 640 Cl 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 641 F phenyl 2-(aminosulfonyl)phenyl 642 F phenyl 2-(methylaminosulfonyl)phenyl 643 F phenyl 1-pyrrolidinocarbonyl 644 F phenyl 2-(methylsulfonyl)phenyl 645 F phenyl 4-morpholino 646 F phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 647 F phenyl 4-morpholinocarbonyl 648 F phenyl 2-methyl-1-imidazolyl 649 F phenyl 5-methyl-1-imidazolyl 650 F phenyl 2-methylsulfonyl-1-imidazolyl 651 F 2-pyridyl 2-(aminosulfonyl)phenyl 652 F 2-pyridyl 2-(methylaminosulfonyl)phenyl 653 F 2-pyridyl 1-pyrrolidinocarbonyl 654 F 2-pyridyl 2-(methylsulfonyl)phenyl 655 F 2-pyridyl 4-morpholino 656 F 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 657 F 2-pyridyl 4-morpholinocarbonyl 658 F 2-pyridyl 2-methyl-1-imidazolyl 659 F 2-pyridyl 5-methyl-1-imidazolyl 660 F 2-pyridyl 2-methylsulfonyl-1-imidazolyl 661 F 3-pyridyl 2-(aminosulfonyl)phenyl 662 F 3-pyridyl 2-(methylaminosulfonyl)phenyl 663 F 3-pyridyl 1-pyrrolidinocarbonyl 664 F 3-pyridyl 2-(methylsulfonyl)phenyl 665 F 3-pyridyl 4-morpholino 666 F 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 667 F 3-pyridyl 4-morpholinocarbonyl 668 F 3-pyridyl 2-methyl-1-imidazolyl 669 F 3-pyridyl 5-methyl-1-imidazolyl 670 F 3-pyridyl 2-methylsulfonyl-1-imidazolyl 671 F 2-pyrimidyl 2-(aminosulfonyl)phenyl 672 F 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 673 F 2-pyrimidyl 1-pyrrolidinocarbonyl 674 F 2-pyrimidyl 2-(methylsulfonyl)phenyl 675 F 2-pyrimidyl 4-morpholino 676 F 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 677 F 2-pyrimidyl 4-morpholinocarbonyl 678 F 2-pyrimidyl 2-methyl-1-imidazolyl 679 F 2-pyrimidyl 5-methyl-1-imidazolyl 680 F 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 681 F 5-pyrimidyl 2-(aminosulfonyl)phenyl 682 F 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 683 F 5-pyrimidyl 1-pyrrolidinocarbonyl 684 F 5-pyrimidyl 2-(methylsulfonyl)phenyl 685 F 5-pyrimidyl 4-morpholino 686 F 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 687 F 5-pyrimidyl 4-morpholinocarbonyl 688 F 5-pyrimidyl 2-methyl-1-imidazolyl 689 F 5-pyrimidyl 5-methyl-1-imidazolyl 690 F 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 691 F 2-Cl-phenyl 2-(aminosulfonyl)phenyl 692 F 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 693 F 2-Cl-phenyl 1-pyrrolidinocarbonyl 694 F 2-Cl-phenyl 2-(methylsulfonyl)phenyl 695 F 2-Cl-phenyl 4-morpholino 696 F 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 697 F 2-Cl-phenyl 4-morpholinocarbonyl 698 F 2-Cl-phenyl 2-methyl-1-imidazolyl 699 F 2-Cl-phenyl 5-methyl-1-imidazolyl 700 F 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 701 F 2-F-phenyl 2-(aminosulfonyl)phenyl 702 F 2-F-phenyl 2-(methylaminosulfonyl)phenyl 703 F 2-F-phenyl 1-pyrrolidinocarbonyl 704 F 2-F-phenyl 2-(methylsulfonyl)phenyl 705 F 2-F-phenyl 4-morpholino 706 F 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 707 F 2-F-phenyl 4-morpholinocarbonyl 708 F 2-F-phenyl 2-methyl-1-imidazolyl 709 F 2-F-phenyl 5-methyl-1-imidazolyl 710 F 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 711 F 2 6-diF-phenyl 2-(aminosulfonyl)phenyl 712 F 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 713 F 2,6-diF-phenyl 1-pyrrolidinocarbonyl 714 F 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 715 F 2,6-diF-phenyl 4-morpholino 716 F 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 717 F 2,6-diF-phenyl 4-morpholinocarbonyl 718 F 2,6-diF-phenyl 2-methyl-1-imidazolyl 719 F 2,6-diF-phenyl 5-methyl-1-imidazolyl 720 F 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 721 CO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 722 CO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 723 CO₂CH₃ phenyl 1-pyrrolidinocarbonyl 724 CO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 725 CO₂CH₃ phenyl 4-morpholino 726 CO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 727 CO₂CH₃ phenyl 4-morpholinocarbonyl 728 CO₂CH₃ phenyl 2-methyl-1-imidazolyl 729 CO₂CH₃ phenyl 5-methyl-1-imidazolyl 730 CO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 731 CO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 732 CO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 733 CO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 734 CO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 735 CO₂CH₃ 2-pyridyl 4-morpholino 736 CO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 737 CO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 738 CO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 739 CO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 740 CO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 741 CO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 742 CO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 743 CO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 744 CO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 745 CO₂CH₃ 3-pyridyl 4-morpholino 746 CO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 747 CO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 748 CO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 749 CO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 750 CO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 751 CO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 752 CO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 753 CO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 754 CO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 755 CO₂CH₃ 2-pyrimidyl 4-morpholino 756 CO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 757 CO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 758 CO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 759 CO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 760 CO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 761 CO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 762 CO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 763 CO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 764 CO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 765 CO₂CH₃ 5-pyrimidyl 4-morpholino 766 CO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 767 CO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 768 CO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 769 CO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 770 CO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 771 CO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 772 CO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 773 CO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 774 CO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 775 CO₂CH₃ 2-Cl-phenyl 4-morpholino 776 CO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 777 CO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 778 CO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 779 CO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 780 CO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 781 CO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 782 CO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 783 CO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 784 CO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 785 CO₂CH₃ 2-F-phenyl 4-morpholino 786 CO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 787 CO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 788 CO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 789 CO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 790 CO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 791 CO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 792 CO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 793 CO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 794 CO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 795 CO₂CH₃ 2,6-diF-phenyl 4-morpholino 796 CO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 797 CO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 798 CO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 799 CO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 800 CO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 801 CH₂OCH₃ phenyl 2-(aminosulfonyl)phenyl 802 CH₂OCH₃ phenyl 2-(methylaminosulfonyl)phenyl 803 CH₂OCH₃ phenyl 1-pyrrolidinocarbonyl 804 CH₂OCH₃ phenyl 2-(methylsulfonyl)phenyl 805 CH₂OCH₃ phenyl 4-morpholino 806 CH₂OCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 807 CH₂OCH₃ phenyl 4-morpholinocarbonyl 808 CH₂OCH₃ phenyl 2-methyl-1-imidazolyl 809 CH₂OCH₃ phenyl 5-methyl-1-imidazolyl 810 CH₂OCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 811 CH₂OCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 812 CH₂OCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 813 CH₂OCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 814 CH₂OCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 815 CH₂OCH₃ 2-pyridyl 4-morpholino 816 CH₂OCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 817 CH₂OCH₃ 2-pyridyl 4-morpholinocarbonyl 818 CH₂OCH₃ 2-pyridyl 2-methyl-1-imidazolyl 819 CH₂OCH₃ 2-pyridyl 5-methyl-1-imidazolyl 820 CH₂OCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 821 CH₂OCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 822 CH₂OCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 823 CH₂OCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 824 CH₂OCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 825 CH₂OCH₃ 3-pyridyl 4-morpholino 826 CH₂OCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 827 CH₂OCH₃ 3-pyridyl 4-morpholinocarbonyl 828 CH₂OCH₃ 3-pyridyl 2-methyl-1-imidazolyl 829 CH₂OCH₃ 3-pyridyl 5-methyl-1-imidazolyl 830 CH₂OCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 831 CH₂OCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 832 CH₂OCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 833 CH₂OCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 834 CH₂OCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 835 CH₂OCH₃ 2-pyrimidyl 4-morpholino 836 CH₂OCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 837 CH₂OCH₃ 2-pyrimidyl 4-morpholinocarbonyl 838 CH₂OCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 839 CH₂OCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 840 CH₂OCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 841 CH₂OCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 842 CH₂OCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 843 CH₂OCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 844 CH₂OCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 845 CH₂OCH₃ 5-pyrimidyl 4-morpholino 846 CH₂OCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 847 CH₂OCH₃ 5-pyrimidyl 4-morpholinocarbonyl 848 CH₂OCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 849 CH₂OCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 850 CH₂OCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 851 CH₂OCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 852 CH₂OCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 853 CH₂OCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 854 CH₂OCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 855 CH₂OCH₃ 2-Cl-phenyl 4-morpholino 856 CH₂OCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 857 CH₂OCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 858 CH₂OCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 859 CH₂OCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 860 CH₂OCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 861 CH₂OCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 862 CH₂OCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 863 CH₂OCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 864 CH₂OCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 865 CH₂OCH₃ 2-F-phenyl 4-morpholino 866 CH₂OCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 867 CH₂OCH₃ 2-F-phenyl 4-morpholinocarbonyl 868 CH₂OCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 869 CH₂OCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 870 CH₂OCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 871 CH₂OCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 872 CH₂OCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 873 CH₂OCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 874 CH₂OCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 875 CH₂OCH₃ 2,6-diF-phenyl 4-morpholino 876 CH₂OCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 877 CH₂OCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 878 CH₂OCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 879 CH₂OCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 880 CH₂OCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 881 CONH₂ phenyl 2-(aminosulfonyl)phenyl 882 CONH₂ phenyl 2-(methylaminosulfonyl)phenyl 883 CONH₂ phenyl 1-pyrrolidinocarbonyl 884 CONH₂ phenyl 2-(methylsulfonyl)phenyl 885 CONH₂ phenyl 4-morpholino 886 CONH₂ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 887 CONH₂ phenyl 4-morpholinocarbonyl 888 CONH₂ phenyl 2-methyl-1-imidazolyl 889 CONH₂ phenyl 5-methyl-1-imidazolyl 890 CONH₂ phenyl 2-methylsulfonyl-1-imidazolyl 891 CONH₂ 2-pyridyl 2-(aminosulfonyl)phenyl 892 CONH₂ 2-pyridyl 2-(methylaminosulfonyl)phenyl 893 CONH₂ 2-pyridyl 1-pyrrolidinocarbonyl 894 CONH₂ 2-pyridyl 2-(methylsulfonyl)phenyl 895 CONH₂ 2-pyridyl 4-morpholino 896 CONH₂ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 897 CONH₂ 2-pyridyl 4-morpholinocarbonyl 898 CONH₂ 2-pyridyl 2-methyl-1-imidazolyl 899 CONH₂ 2-pyridyl 5-methyl-1-imidazolyl 900 CONH₂ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 901 CONH₂ 3-pyridyl 2-(aminosulfonyl)phenyl 902 CONH₂ 3-pyridyl 2-(methylaminosulfonyl)phenyl 903 CONH₂ 3-pyridyl 1-pyrrolidinocarbonyl 904 CONH₂ 3-pyridyl 2-(methylsulfonyl)phenyl 905 CONH₂ 3-pyridyl 4-morpholino 906 CONH₂ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 907 CONH₂ 3-pyridyl 4-morpholinocarbonyl 908 CONH₂ 3-pyridyl 2-methyl-1-imidazolyl 909 CONH₂ 3-pyridyl 5-methyl-1-imidazolyl 910 CONH₂ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 911 CONH₂ 2-pyrimidyl 2-(aminosulfonyl)phenyl 912 CONH₂ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 913 CONH₂ 2-pyrimidyl 1-pyrrolidinocarbonyl 914 CONH₂ 2-pyrimidyl 2-(methylsulfonyl)phenyl 915 CONH₂ 2-pyrimidyl 4-morpholino 916 CONH₂ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 917 CONH₂ 2-pyrimidyl 4-morpholinocarbonyl 918 CONH₂ 2-pyrimidyl 2-methyl-1-imidazolyl 919 CONH₂ 2-pyrimidyl 5-methyl-1-imidazolyl 920 CONH₂ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 921 CONH₂ 5-pyrimidyl 2-(aminosulfonyl)phenyl 922 CONH₂ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 923 CONH₂ 5-pyrimidyl 1-pyrrolidinocarbonyl 924 CONH₂ 5-pyrimidyl 2-(methylsulfonyl)phenyl 925 CONH₂ 5-pyrimidyl 4-morpholino 926 CONH₂ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 927 CONH₂ 5-pyrimidyl 4-morpholinocarbonyl 928 CONH₂ 5-pyrimidyl 2-methyl-1-imidazolyl 929 CONH₂ 5-pyrimidyl 5-methyl-1-imidazolyl 930 CONH₂ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 931 CONH₂ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 932 CONH₂ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 933 CONH₂ 2-Cl-phenyl 1-pyrrolidinocarbonyl 934 CONH₂ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 935 CONH₂ 2-Cl-phenyl 4-morpholino 936 CONH₂ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 937 CONH₂ 2-Cl-phenyl 4-morpholinocarbonyl 938 CONH₂ 2-Cl-phenyl 2-methyl-1-imidazolyl 939 CONH₂ 2-Cl-phenyl 5-methyl-1-imidazolyl 940 CONH₂ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 941 CONH₂ 2-F-phenyl 2-(aminosulfonyl)phenyl 942 CONH₂ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 943 CONH₂ 2-F-phenyl 1-pyrrolidinocarbonyl 944 CONH₂ 2-F-phenyl 2-(methylsulfonyl)phenyl 945 CONH₂ 2-F-phenyl 4-morpholino 946 CONH₂ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 947 CONH₂ 2-F-phenyl 4-morpholinocarbonyl 948 CONH₂ 2-F-phenyl 2-methyl-1-imidazolyl 949 CONH₂ 2-F-phenyl 5-methyl-1-imidazolyl 950 CONH₂ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 951 CONH₂ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 952 CONH₂ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 953 CONH₂ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 954 CONH₂ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 955 CONH₂ 2,6-diF-phenyl 4-morpholino 956 CONH₂ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 957 CONH₂ 2,6-diF-phenyl 4-morpholinocarbonyl 958 CONH₂ 2,6-diF-phenyl 2-methyl-1-imidazolyl 959 CONH₂ 2,6-diF-phenyl 5-methyl-1-imidazolyl 960 CONH₂ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl

TABLE 3

Ex # A B  1 phenyl 2-(aminosulfonyl)phenyl  2 phenyl 2-(methylaminosulfonyl)phenyl  3 phenyl 1-pyrrolidinocarbonyl  4 phenyl 2-(methylsulfonyl)phenyl  5 phenyl 4-morpholino  6 phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  7 phenyl 4-morpholinocarbonyl  8 phenyl 2-methyl-1-imidazolyl  9 phenyl 5-methyl-1-imidazolyl 10 phenyl 2-methylsulfonyl-1-imidazolyl 11 2-pyridyl 2-(aminosulfonyl)phenyl 12 2-pyridyl 2-(methylaminosulfonyl)phenyl 13 2-pyridyl 1-pyrrolidinocarbonyl 14 2-pyridyl 2-(methylsulfonyl)phenyl 15 2-pyridyl 4-morpholino 16 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 17 2-pyridyl 4-morpholinocarbonyl 18 2-pyridyl 2-methyl-1-imidazolyl 19 2-pyridyl 5-methyl-1-imidazolyl 20 2-pyridyl 2-methylsulfonyl-1-imidazolyl 21 3-pyridyl 2-(aminosulfonyl)phenyl 22 3-pyridyl 2-(methylaminosulfonyl)phenyl 23 3-pyridyl 1-pyrrolidinocarbonyl 24 3-pyridyl 2-(methylsulfonyl)phenyl 25 3-pyridyl 4-morpholino 26 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 27 3-pyridyl 4-morpholinocarbonyl 28 3-pyridyl 2-methyl-1-imidazolyl 29 3-pyridyl 5-methyl-1-imidazolyl 30 3-pyridyl 2-methylsulfonyl-1-imidazolyl 31 2-pyrimidyl 2-(aminosulfonyl)phenyl 32 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 33 2-pyrimidyl 1-pyrrolidinocarbonyl 34 2-pyrimidyl 2-(methylsulfonyl)phenyl 35 2-pyrimidyl 4-morpholino 36 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 37 2-pyrimidyl 4-morpholinocarbonyl 38 2-pyrimidyl 2-methyl-1-imidazolyl 39 2-pyrimidyl 5-methyl-1-imidazolyl 40 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 41 5-pyrimidyl 2-(aminosulfonyl)phenyl 42 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 43 5-pyrimidyl 1-pyrrolidinocarbonyl 44 5-pyrimidyl 2-(methylsulfonyl)phenyl 45 5-pyrimidyl 4-morpholino 46 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 47 5-pyrimidyl 4-morpholinocarbonyl 48 5-pyrimidyl 2-methyl-1-imidazolyl 49 5-pyrimidyl 5-methyl-1-imidazolyl 50 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 51 2-Cl-phenyl 2-(aminosulfonyl)phenyl 52 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 53 2-Cl-phenyl 1-pyrrolidinocarbonyl 54 2-Cl-phenyl 2-(methylsulfonyl)phenyl 55 2-Cl-phenyl 4-morpholino 56 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 57 2-Cl-phenyl 4-morpholinocarbonyl 58 2-Cl-phenyl 2-methyl-1-imidazolyl 59 2-Cl-phenyl 5-methyl-1-imidazolyl 60 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 61 2-F-phenyl 2-(aminosulfonyl)phenyl 62 2-F-phenyl 2-(methylaminosulfonyl)phenyl 63 2-F-phenyl 1-pyrrolidinocarbonyl 64 2-F-phenyl 2-(methylsulfonyl)phenyl 65 2-F-phenyl 4-morpholino 66 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 67 2-F-phenyl 4-morpholinocarbonyl 68 2-F-phenyl 2-methyl-1-imidazolyl 69 2-F-phenyl 5-methyl-1-imidazolyl 70 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 71 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 72 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 73 2,6-diF-phenyl 1-pyrrolidinocarbonyl 74 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 75 2,6-diF-phenyl 4-morpholino 76 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 77 2,6-diF-phenyl 4-morpholinocarbonyl 78 2,6-diF-phenyl 2-methyl-1-imidazolyl 79 2,6-diF-phenyl 5-methyl-1-imidazolyl 80 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl

TABLE 4

For each example, DE is: (A) pyridin-4-yl-CH₂, (B) 2-amino-pyrimidin-4-yl, (C) 6-amino-pyridin-2-yl, (D) 3-amidino-4-F-phenyl, or (E) N-amidino-3-piperidinyl. Ex # R^(1a) A B  1 CH₃ phenyl 2-(aminosulfonyl)phenyl  2 CH₃ phenyl 2-(methylaminosulfonyl)phenyl  3 CH₃ phenyl 1-pyrrolidinocarbonyl  4 CH₃ phenyl 2-(methylsulfonyl)phenyl  5 CH₃ phenyl 4-morpholino  6 CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  7 CH₃ phenyl 4-morpholinocarbonyl  8 CH₃ phenyl 2-methyl-1-imidazolyl  9 CH₃ phenyl 5-methyl-1-imidazolyl  10 CH₃ phenyl 2-methylsulfonyl-1-imidazolyl  11 CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl  12 CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl  13 CH₃ 2-pyridyl 1-pyrrolidinocarbonyl  14 CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl  15 CH₃ 2-pyridyl 4-morpholino  16 CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  17 CH₃ 2-pyridyl 4-morpholinocarbonyl  18 CH₃ 2-pyridyl 2-methyl-1-imidazolyl  19 CH₃ 2-pyridyl 5-methyl-1-imidazolyl  20 CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl  21 CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl  22 CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl  23 CH₃ 3-pyridyl 1-pyrrolidinocarbonyl  24 CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl  25 CH₃ 3-pyridyl 4-morpholino  26 CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  27 CH₃ 3-pyridyl 4-morpholinocarbonyl  28 CH₃ 3-pyridyl 2-methyl-1-imidazolyl  29 CH₃ 3-pyridyl 5-methyl-1-imidazolyl  30 CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl  31 CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl  32 CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl  33 CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl  34 CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl  35 CH₃ 2-pyrimidyl 4-morpholino  36 CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  37 CH₃ 2-pyrimidyl 4-morpholinocarbonyl  38 CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl  39 CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl  40 CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl  41 CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl  42 CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl  43 CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl  44 CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl  45 CH₃ 5-pyrimidyl 4-morpholino  46 CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  47 CH₃ 5-pyrimidyl 4-morpholinocarbonyl  48 CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl  49 CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl  50 CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl  51 CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl  52 CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl  53 CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl  54 CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl  55 CH₃ 2-Cl-phenyl 4-morpholino  56 CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  57 CH₃ 2-Cl-phenyl 4-morpholinocarbonyl  58 CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl  59 CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl  60 CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl  61 CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl  62 CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl  63 CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl  64 CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl  65 CH₃ 2-F-phenyl 4-morpholino  66 CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  67 CH₃ 2-F-phenyl 4-morpholinocarbonyl  68 CH₃ 2-F-phenyl 2-methyl-1-imidazolyl  69 CH₃ 2-F-phenyl 5-methyl-1-imidazolyl  70 CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl  71 CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl  72 CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl  73 CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl  74 CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl  75 CH₃ 2,6-diF-phenyl 4-morpholino  76 CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  77 CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl  78 CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl  79 CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl  80 CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl  81 CH₂CH₃ phenyl 2-(aminosulfonyl)phenyl  82 CH₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl  83 CH₂CH₃ phenyl 1-pyrrolidinocarbonyl  84 CH₂CH₃ phenyl 2-(methylsulfonyl)phenyl  85 CH₂CH₃ phenyl 4-morpholino  86 CH₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  87 CH₂CH₃ phenyl 4-morpholinocarbonyl  88 CH₂CH₃ phenyl 2-methyl-1-imidazolyl  89 CH₂CH₃ phenyl 5-methyl-1-imidazolyl  90 CH₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl  91 CH₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl  92 CH₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl  93 CH₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl  94 CH₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl  95 CH₂CH₃ 2-pyridyl 4-morpholino  96 CH₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  97 CH₂CH₃ 2-pyridyl 4-morpholinocarbonyl  98 CH₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl  99 CH₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 100 CH₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 101 CH₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 102 CH₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 103 CH₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 104 CH₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 105 CH₂CH₃ 3-pyridyl 4-morpholino 106 CH₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 107 CH₂CH₃ 3-pyridyl 4-morpholinocarbonyl 108 CH₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 109 CH₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 110 CH₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 111 CH₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 112 CH₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 113 CH₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 114 CH₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 115 CH₂CH₃ 2-pyrimidyl 4-morpholino 116 CH₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 117 CH₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 118 CH₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 119 CH₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 120 CH₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 121 CH₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 122 CH₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 123 CH₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 124 CH₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 125 CH₂CH₃ 5-pyrimidyl 4-morpholino 126 CH₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 127 CH₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 128 CH₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 129 CH₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 130 CH₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 131 CH₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 132 CH₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 133 CH₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 134 CH₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 135 CH₂CH₃ 2-Cl-phenyl 4-morpholino 136 CH₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 137 CH₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 138 CH₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 139 CH₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 140 CH₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 141 CH₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 142 CH₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 143 CH₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 144 CH₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 145 CH₂CH₃ 2-F-phenyl 4-morpholino 146 CH₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 147 CH₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 148 CH₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 149 CH₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 150 CH₂CH₃ 2-F-phenyl 2-methylsulfonyl-l-imidazolyl 151 CH₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 152 CH₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 153 CH₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 154 CH₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 155 CH₂CH₃ 2,6-diF-phenyl 4-morpholino 156 CH₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 157 CH₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 158 CH₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 159 CH₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 160 CH₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 161 CF₃ phenyl 2-(aminosulfonyl)phenyl 162 CF₃ phenyl 2-(methylaminosulfonyl)phenyl 163 CF₃ phenyl 1-pyrrolidinocarbonyl 164 CF₃ phenyl 2-(methylsulfonyl)phenyl 165 CF₃ phenyl 4-morpholino 166 CF₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 167 CF₃ phenyl 4-morpholinocarbonyl 168 CF₃ phenyl 2-methyl-1-imidazolyl 169 CF₃ phenyl 5-methyl-1-imidazolyl 170 CF₃ phenyl 2-methylsulfonyl-1-imidazolyl 171 CF₃ 2-pyridyl 2-(aminosulfonyl)phenyl 172 CF₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 173 CF₃ 2-pyridyl 1-pyrrolidinocarbonyl 174 CF₃ 2-pyridyl 2-(methylsulfonyl)phenyl 175 CF₃ 2-pyridyl 4-morpholino 176 CF₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 177 CF₃ 2-pyridyl 4-morpholinocarbonyl 178 CF₃ 2-pyridyl 2-methyl-1-imidazolyl 179 CF₃ 2-pyridyl 5-methyl-1-imidazolyl 180 CF₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 181 CF₃ 3-pyridyl 2-(aminosulfonyl)phenyl 182 CF₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 183 CF₃ 3-pyridyl 1-pyrrolidinocarbonyl 184 CF₃ 3-pyridyl 2-(methylsulfonyl)phenyl 185 CF₃ 3-pyridyl 4-morpholino 186 CF₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 187 CF₃ 3-pyridyl 4-morpholinocarbonyl 188 CF₃ 3-pyridyl 2-methyl-1-imidazolyl 189 CF₃ 3-pyridyl 5-methyl-1-imidazolyl 190 CF₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 191 CF₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 192 CF₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 193 CF₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 194 CF₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 195 CF₃ 2-pyrimidyl 4-morpholino 196 CF₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 197 CF₃ 2-pyrimidyl 4-morpholinocarbonyl 198 CF₃ 2-pyrimidyl 2-methyl-1-imidazolyl 199 CF₃ 2-pyrimidyl 5-methyl-1-imidazolyl 200 CF₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 201 CF₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 202 CF₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 203 CF₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 204 CF₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 205 CF₃ 5-pyrimidyl 4-morpholino 206 CF₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 207 CF₃ 5-pyrimidyl 4-morpholinocarbonyl 208 CF₃ 5-pyrimidyl 2-methyl-1-imidazolyl 209 CF₃ 5-pyrimidyl 5-methyl-1-imidazolyl 210 CF₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 211 CF₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 212 CF₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 213 CF₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 214 CF₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 215 CF₃ 2-Cl-phenyl 4-morpholino 216 CF₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 217 CF₃ 2-Cl-phenyl 4-morpholinocarbonyl 218 CF₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 219 CF₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 220 CF₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 221 CF₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 222 CF₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 223 CF₃ 2-F-phenyl 1-pyrrolidinocarbonyl 224 CF₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 225 CF₃ 2-F-phenyl 4-morpholino 226 CF₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 227 CF₃ 2-F-phenyl 4-morpholinocarbonyl 228 CF₃ 2-F-phenyl 2-methyl-1-imidazolyl 229 CF₃ 2-F-phenyl 5-methyl-1-imidazolyl 230 CF₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 231 CF₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 232 CF₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 233 CF₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 234 CF₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 235 CF₃ 2,6-diF-phenyl 4-morpholino 236 CF₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 237 CF₃ 2,6-diF-phenyl 4-morpholinocarbonyl 238 CF₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 239 CF₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 240 CF₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 241 SCH₃ phenyl 2-(aminosulfonyl)phenyl 242 SCH₃ phenyl 2-(methylaminosulfonyl)phenyl 243 SCH₃ phenyl 1-pyrrolidinocarbonyl 244 SCH₃ phenyl 2-(methylsulfonyl)phenyl 245 SCH₃ phenyl 4-morpholino 246 SCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 247 SCH₃ phenyl 4-morpholinocarbonyl 248 SCH₃ phenyl 2-methyl-1-imidazolyl 249 SCH₃ phenyl 5-methyl-1-imidazolyl 250 SCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 251 SCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 252 SCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 253 SCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 254 SCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 255 SCH₃ 2-pyridyl 4-morpholino 256 SCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 257 SCH₃ 2-pyridyl 4-morpholinocarbonyl 258 SCH₃ 2-pyridyl 2-methyl-1-imidazolyl 259 SCH₃ 2-pyridyl 5-methyl-1-imidazolyl 260 SCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 261 SCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 262 SCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 263 SCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 264 SCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 265 SCH₃ 3-pyridyl 4-morpholino 266 SCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 267 SCH₃ 3-pyridyl 4-morpholinocarbonyl 268 SCH₃ 3-pyridyl 2-methyl-1-imidazolyl 269 SCH₃ 3-pyridyl 5-methyl-1-imidazolyl 270 SCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 271 SCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 272 SCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 273 SCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 274 SCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 275 SCH₃ 2-pyrimidyl 4-morpholino 276 SCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 277 SCH₃ 2-pyrimidyl 4-morpholinocarbonyl 278 SCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 279 SCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 280 SCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 281 SCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 282 SCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 283 SCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 284 SCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 285 SCH₃ 5-pyrimidyl 4-morpholino 286 SCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 287 SCH₃ 5-pyrimidyl 4-morpholinocarbonyl 288 SCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 289 SCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 290 SCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 291 SCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 292 SCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 293 SCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 294 SCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 295 SCH₃ 2-Cl-phenyl 4-morpholino 296 SCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 297 SCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 298 SCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 299 SCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 300 SCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 301 SCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 302 SCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 303 SCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 304 SCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 305 SCH₃ 2-F-phenyl 4-morpholino 306 SCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 307 SCH₃ 2-F-phenyl 4-morpholinocarbonyl 308 SCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 309 SCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 310 SCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 311 SCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 312 SCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 313 SCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 314 SCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 315 SCH₃ 2,6-diF-phenyl 4-morpholino 316 SCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 317 SCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 318 SCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 319 SCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 320 SCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 321 SOCH₃ phenyl 2-(aminosulfonyl)phenyl 322 SOCH₃ phenyl 2-(methylaminosulfonyl)phenyl 323 SOCH₃ phenyl 1-pyrrolidinocarbonyl 324 SOCH₃ phenyl 2-(methylsulfonyl)phenyl 325 SOCH₃ phenyl 4-morpholino 326 SOCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 327 SOCH₃ phenyl 4-morpholinocarbonyl 328 SOCH₃ phenyl 2-methyl-1-imidazolyl 329 SOCH₃ phenyl 5-methyl-1-imidazolyl 330 SOCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 331 SOCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 332 SOCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 333 SOCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 334 SOCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 335 SOCH₃ 2-pyridyl 4-morpholino 336 SOCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 337 SOCH₃ 2-pyridyl 4-morpholinocarbonyl 338 SOCH₃ 2-pyridyl 2-methyl-1-imidazolyl 339 SOCH₃ 2-pyridyl 5-methyl-1-imidazolyl 340 SOCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 341 SOCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 342 SOCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 343 SOCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 344 SOCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 345 SOCH₃ 3-pyridyl 4-morpholino 346 SOCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 347 SOCH₃ 3-pyridyl 4-morpholinocarbonyl 348 SOCH₃ 3-pyridyl 2-methyl-1-imidazolyl 349 SOCH₃ 3-pyridyl 5-methyl-1-imidazolyl 350 SOCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 351 SOCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 352 SOCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 353 SOCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 354 SOCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 355 SOCH₃ 2-pyrimidyl 4-morpholino 356 SOCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 357 SOCH₃ 2-pyrimidyl 4-morpholinocarbonyl 358 SOCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 359 SOCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 360 SOCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 361 SOCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 362 SOCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 363 SOCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 364 SOCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 365 SOCH₃ 5-pyrimidyl 4-morpholino 366 SOCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 367 SOCH₃ 5-pyrimidyl 4-morpholinocarbonyl 368 SOCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 369 SOCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 370 SOCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 371 SOCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 372 SOCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 373 SOCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 374 SOCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 375 SOCH₃ 2-Cl-phenyl 4-morpholino 376 SOCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 377 SOCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 378 SOCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 379 SOCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 380 SOCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 381 SOCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 382 SOCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 383 SOCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 384 SOCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 385 SOCH₃ 2-F-phenyl 4-morpholino 386 SOCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 387 SOCH₃ 2-F-phenyl 4-morpholinocarbonyl 388 SOCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 389 SOCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 390 SOCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 391 SOCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 392 SOCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 393 SOCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 394 SOCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 395 SOCH₃ 2,6-diF-phenyl 4-morpholino 396 SOCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 397 SOCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 398 SOCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 399 SOCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 400 SOCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 401 SO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 402 SO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 403 SO₂CH₃ phenyl 1-pyrrolidinocarbonyl 404 SO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 405 SO₂CH₃ phenyl 4-morpholino 406 SO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 407 SO₂CH₃ phenyl 4-morpholinocarbonyl 408 SO₂CH₃ phenyl 2-methyl-1-imidazolyl 409 SO₂CH₃ phenyl 5-methyl-1-imidazolyl 410 SO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 411 SO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 412 SO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 413 SO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 414 SO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 415 SO₂CH₃ 2-pyridyl 4-morpholino 416 SO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 417 SO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 418 SO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 419 SO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 420 SO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 421 SO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 422 SO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 423 SO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 424 SO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 425 SO₂CH₃ 3-pyridyl 4-morpholino 426 SO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 427 SO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 428 SO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 429 SO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 430 SO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 431 SO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 432 SO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 433 SO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 434 SO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 435 SO₂CH₃ 2-pyrimidyl 4-morpholino 436 SO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 437 SO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 438 SO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 439 SO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 440 SO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 441 SO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 442 SO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 443 SO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 444 SO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 445 SO₂CH₃ 5-pyrimidyl 4-morpholino 446 SO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 447 SO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 448 SO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 449 SO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 450 SO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 451 SO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 452 SO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 453 SO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 454 SO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 455 SO₂CH₃ 2-Cl-phenyl 4-morpholino 456 SO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 457 SO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 458 SO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 459 SO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 460 SO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 461 SO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 462 SO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 463 SO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 464 SO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 465 SO₂CH₃ 2-F-phenyl 4-morpholino 466 SO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 467 SO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 468 SO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 469 SO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 470 SO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 471 SO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 472 SO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 473 SO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 474 SO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 475 SO₂CH₃ 2,6-diF-phenyl 4-morpholino 476 SO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 477 SO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 478 SO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 479 SO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 480 SO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 481 CH₂NH— phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 482 CH₂NH— phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 483 CH₂NH— phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 484 CH₂NH— phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 485 CH₂NH— phenyl 4-morpholino SO₂CH₃ 486 CH₂NH— phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 487 CH₂NH— phenyl 4-morpholinocarbonyl SO₂CH₃ 488 CH₂NH— phenyl 2-methyl-1-imidazolyl SO₂CH₃ 489 CH₂NH— phenyl 5-methyl-1-imidazolyl SO₂CH₃ 490 CH₂NH— phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 491 CH₂NH— 2-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 492 CH₂NH— 2-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 493 CH₂NH— 2-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 494 CH₂NH— 2-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 495 CH₂NH— 2-pyridyl 4-morpholino SO₂CH₃ 496 CH₂NH— 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 497 CH₂NH— 2-pyridyl 4-morpholinocarbonyl SO₂CH₃ 498 CH₂NH— 2-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 499 CH₂NH— 2-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 500 CH₂NH— 2-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 501 CH₂NH— 3-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 502 CH₂NH— 3-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 503 CH₂NH— 3-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 504 CH₂NH— 3-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 505 CH₂NH— 3-pyridyl 4-morpholino SO₂CH₃ 506 CH₂NH— 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 507 CH₂NH— 3-pyridyl 4-morpholinocarbonyl SO₂CH₃ 508 CH₂NH— 3-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 509 CH₂NH— 3-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 510 CH₂NH— 3-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 511 CH₂NH— 2-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 512 CH₂NH— 2-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 513 CH₂NH— 2-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 514 CH₂NH— 2-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 515 CH₂NH— 2-pyrimidyl 4-morpholino SO₂CH₃ 516 CH₂NH— 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 517 CH₂NH— 2-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 518 CH₂NH— 2-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 519 CH₂NH— 2-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 520 CH₂NH— 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 521 CH₂NH— 5-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 522 CH₂NH— 5-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 523 CH₂NH— 5-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 524 CH₂NH— 5-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 525 CH₂NH— 5-pyrimidyl 4-morpholino SO₂CH₃ 526 CH₂NH— 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 527 CH₂NH— 5-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 528 CH₂NH— 5-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 529 CH₂NH— 5-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 530 CH₂NH— 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 531 CH₂NH— 2-Cl-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 532 CH₂NH— 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 533 CH₂NH— 2-Cl-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 534 CH₂NH— 2-Cl-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 535 CH₂NH— 2-Cl-phenyl 4-morpholino SO₂CH₃ 536 CH₂NH— 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 537 CH₂NH— 2-Cl-phenyl 4-morpholinocarbonyl SO₂CH₃ 538 CH₂NH— 2-Cl-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 539 CH₂NH— 2-Cl-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 540 CH₂NH— 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 541 CH₂NH— 2-F-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 542 CH₂NH— 2-F-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 543 CH₂NH— 2-F-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 544 CH₂NH— 2-F-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 545 CH₂NH— 2-F-phenyl 4-morpholino SO₂CH₃ 546 CH₂NH— 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 547 CH₂NH— 2-F-phenyl 4-morpholinocarbonyl SO₂CH₃ 548 CH₂NH— 2-F-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 549 CH₂NH— 2-F-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 550 CH₂NH— 2-F-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 551 CH₂NH— 2,6-diF-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 552 CH₂NH— 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 553 CH₂NH— 2,6-diF-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 554 CH₂NH— 2,6-diF-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 555 CH₂NH— 2,6-diF-phenyl 4-morpholino SO₂CH₃ 556 CH₂NH— 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 557 CH₂NH— 2,6-diF-phenyl 4-morpholinocarbonyl SO₂CH₃ 558 CH₂NH— 2,6-diF-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 559 CH₂NH— 2,6-diF-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 560 CH₂NH— 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 561 Cl phenyl 2-(aminosulfonyl)phenyl 562 Cl phenyl 2-(methylaminosulfonyl)phenyl 563 Cl phenyl 1-pyrrolidinocarbonyl 564 Cl phenyl 2-(methylsulfonyl)phenyl 565 Cl phenyl 4-morpholino 566 Cl phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 567 Cl phenyl 4-morpholinocarbonyl 568 Cl phenyl 2-methyl-1-imidazolyl 569 Cl phenyl 5-methyl-1-imidazolyl 570 Cl phenyl 2-methylsulfonyl-1-imidazolyl 571 Cl 2-pyridyl 2-(aminosulfonyl)phenyl 572 Cl 2-pyridyl 2-(methylaminosulfonyl)phenyl 573 Cl 2-pyridyl 1-pyrrolidinocarbonyl 574 Cl 2-pyridyl 2-(methylsulfonyl)phenyl 575 Cl 2-pyridyl 4-morpholino 576 Cl 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 577 Cl 2-pyridyl 4-morpholinocarbonyl 578 Cl 2-pyridyl 2-methyl-1-imidazolyl 579 Cl 2-pyridyl 5-methyl-1-imidazolyl 580 Cl 2-pyridyl 2-methylsulfonyl-1-imidazolyl 581 Cl 3-pyridyl 2-(aminosulfonyl)phenyl 582 Cl 3-pyridyl 2-(methylaminosulfonyl)phenyl 583 Cl 3-pyridyl 1-pyrrolidinocarbonyl 584 Cl 3-pyridyl 2-(methylsulfonyl)phenyl 585 Cl 3-pyridyl 4-morpholino 586 Cl 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 587 Cl 3-pyridyl 4-morpholinocarbonyl 588 Cl 3-pyridyl 2-methyl-1-imidazolyl 589 Cl 3-pyridyl 5-methyl-1-imidazolyl 590 Cl 3-pyridyl 2-methylsulfonyl-1-imidazolyl 591 Cl 2-pyrimidyl 2-(aminosulfonyl)phenyl 592 Cl 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 593 Cl 2-pyrimidyl 1-pyrrolidinocarbonyl 594 Cl 2-pyrimidyl 2-(methylsulfonyl)phenyl 595 Cl 2-pyrimidyl 4-morpholino 596 Cl 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 597 Cl 2-pyrimidyl 4-morpholinocarbonyl 598 Cl 2-pyrimidyl 2-methyl-1-imidazolyl 599 Cl 2-pyrimidyl 5-methyl-1-imidazolyl 600 Cl 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 601 Cl 5-pyrimidyl 2-(aminosulfonyl)phenyl 602 Cl 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 603 Cl 5-pyrimidyl 1-pyrrolidinocarbonyl 604 Cl 5-pyrimidyl 2-(methylsulfonyl)phenyl 605 Cl 5-pyrimidyl 4-morpholino 606 Cl 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 607 Cl 5-pyrimidyl 4-morpholinocarbonyl 608 Cl 5-pyrimidyl 2-methyl-1-imidazolyl 609 Cl 5-pyrimidyl 5-methyl-1-imidazolyl 610 Cl 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 611 Cl 2-Cl-phenyl 2-(aminosulfonyl)phenyl 612 Cl 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 613 Cl 2-Cl-phenyl 1-pyrrolidinocarbonyl 614 Cl 2-Cl-phenyl 2-(methylsulfonyl)phenyl 615 Cl 2-Cl-phenyl 4-morpholino 616 Cl 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 617 Cl 2-Cl-phenyl 4-morpholinocarbonyl 618 Cl 2-Cl-phenyl 2-methyl-1-imidazolyl 619 Cl 2-Cl-phenyl 5-methyl-1-imidazolyl 620 Cl 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 621 Cl 2-F-phenyl 2-(aminosulfonyl)phenyl 622 Cl 2-F-phenyl 2-(methylaminosulfonyl)phenyl 623 Cl 2-F-phenyl 1-pyrrolidinocarbonyl 624 Cl 2-F-phenyl 2-(methylsulfonyl)phenyl 625 Cl 2-F-phenyl 4-morpholino 626 Cl 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 627 Cl 2-F-phenyl 4-morpholinocarbonyl 628 Cl 2-F-phenyl 2-methyl-1-imidazolyl 629 Cl 2-F-phenyl 5-methyl-1-imidazolyl 630 Cl 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 631 Cl 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 632 Cl 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 633 Cl 2,6-diF-phenyl 1-pyrrolidinocarbonyl 634 Cl 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 635 Cl 2,6-diF-phenyl 4-morpholino 636 Cl 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 637 Cl 2,6-diF-phenyl 4-morpholinocarbonyl 638 Cl 2,6-diF-phenyl 2-methyl-1-imidazolyl 639 Cl 2,6-diF-phenyl 5-methyl-1-imidazolyl 640 Cl 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 641 F phenyl 2-(aminosulfonyl)phenyl 642 F phenyl 2-(methylaminosulfonyl)phenyl 643 F phenyl 1-pyrrolidinocarbonyl 644 F phenyl 2-(methylsulfonyl)phenyl 645 F phenyl 4-morpholino 646 F phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 647 F phenyl 4-morpholinocarbonyl 648 F phenyl 2-methyl-1-imidazolyl 649 F phenyl 5-methyl-1-imidazolyl 650 F phenyl 2-methylsulfonyl-1-imidazolyl 651 F 2-pyridyl 2-(aminosulfonyl)phenyl 652 F 2-pyridyl 2-(methylaminosulfonyl)phenyl 653 F 2-pyridyl 1-pyrrolidinocarbonyl 654 F 2-pyridyl 2-(methylsulfonyl)phenyl 655 F 2-pyridyl 4-morpholino 656 F 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 657 F 2-pyridyl 4-morpholinocarbonyl 658 F 2-pyridyl 2-methyl-1-imidazolyl 659 F 2-pyridyl 5-methyl-1-imidazolyl 660 F 2-pyridyl 2-methylsulfonyl-1-imidazolyl 661 F 3-pyridyl 2-(aminosulfonyl)phenyl 662 F 3-pyridyl 2-(methylaminosulfonyl)phenyl 663 F 3-pyridyl 1-pyrrolidinocarbonyl 664 F 3-pyridyl 2-(methylsulfonyl)phenyl 665 F 3-pyridyl 4-morpholino 666 F 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 667 F 3-pyridyl 4-morpholinocarbonyl 668 F 3-pyridyl 2-methyl-1-imidazolyl 669 F 3-pyridyl 5-methyl-1-imidazolyl 670 F 3-pyridyl 2-methylsulfonyl-1-imidazolyl 671 F 2-pyrimidyl 2-(aminosulfonyl)phenyl 672 F 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 673 F 2-pyrimidyl 1-pyrrolidinocarbonyl 674 F 2-pyrimidyl 2-(methylsulfonyl)phenyl 675 F 2-pyrimidyl 4-morpholino 676 F 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 677 F 2-pyrimidyl 4-morpholinocarbonyl 678 F 2-pyrimidyl 2-methyl-1-imidazolyl 679 F 2-pyrimidyl 5-methyl-1-imidazolyl 680 F 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 681 F 5-pyrimidyl 2-(aminosulfonyl)phenyl 682 F 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 683 F 5-pyrimidyl 1-pyrrolidinocarbonyl 684 F 5-pyrimidyl 2-(methylsulfonyl)phenyl 685 F 5-pyrimidyl 4-morpholino 686 F 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 687 F 5-pyrimidyl 4-morpholinocarbonyl 688 F 5-pyrimidyl 2-methyl-1-imidazolyl 689 F 5-pyrimidyl 5-methyl-1-imidazolyl 690 F 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 691 F 2-Cl-phenyl 2-(aminosulfonyl)phenyl 692 F 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 693 F 2-Cl-phenyl 1-pyrrolidinocarbonyl 694 F 2-Cl-phenyl 2-(methylsulfonyl)phenyl 695 F 2-Cl-phenyl 4-morpholino 696 F 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 697 F 2-Cl-phenyl 4-morpholinocarbonyl 698 F 2-Cl-phenyl 2-methyl-1-imidazolyl 699 F 2-Cl-phenyl 5-methyl-1-imidazolyl 700 F 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 701 F 2-F-phenyl 2-(aminosulfonyl)phenyl 702 F 2-F-phenyl 2-(methylaminosulfonyl)phenyl 703 F 2-F-phenyl 1-pyrrolidinocarbonyl 704 F 2-F-phenyl 2-(methylsulfonyl)phenyl 705 F 2-F-phenyl 4-morpholino 706 F 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 707 F 2-F-phenyl 4-morpholinocarbonyl 708 F 2-F-phenyl 2-methyl-1-imidazolyl 709 F 2-F-phenyl 5-methyl-1-imidazolyl 710 F 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 711 F 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 712 F 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 713 F 2,6-diF-phenyl 1-pyrrolidinocarbonyl 714 F 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 715 F 2,6-diF-phenyl 4-morpholino 716 F 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 717 F 2,6-diF-phenyl 4-morpholinocarbonyl 718 F 2,6-diF-phenyl 2-methyl-1-imidazolyl 719 F 2,6-diF-phenyl 5-methyl-1-imidazolyl 720 F 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 721 CO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 722 CO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 723 CO₂CH₃ phenyl 1-pyrrolidinocarbonyl 724 CO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 725 CO₂CH₃ phenyl 4-morpholino 726 CO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 727 CO₂CH₃ phenyl 4-morpholinocarbonyl 728 CO₂CH₃ phenyl 2-methyl-1-imidazolyl 729 CO₂CH₃ phenyl 5-methyl-1-imidazolyl 730 CO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 731 CO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 732 CO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 733 CO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 734 CO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 735 CO₂CH₃ 2-pyridyl 4-morpholino 736 CO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 737 CO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 738 CO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 739 CO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 740 CO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 741 CO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 742 CO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 743 CO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 744 CO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 745 CO₂CH₃ 3-pyridyl 4-morpholino 746 CO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 747 CO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 748 CO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 749 CO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 750 CO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 751 CO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 752 CO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 753 CO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 754 CO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 755 CO₂CH₃ 2-pyrimidyl 4-morpholino 756 CO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 757 CO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 758 CO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 759 CO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 760 CO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 761 CO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 762 CO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 763 CO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 764 CO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 765 CO₂CH₃ 5-pyrimidyl 4-morpholino 766 CO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 767 CO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 768 CO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 769 CO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 770 CO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 771 CO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 772 CO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 773 CO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 774 CO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 775 CO₂CH₃ 2-Cl-phenyl 4-morpholino 776 CO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 777 CO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 778 CO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 779 CO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 780 CO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 781 CO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 782 CO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 783 CO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 784 CO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 785 CO₂CH₃ 2-F-phenyl 4-morpholino 786 CO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 787 CO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 788 CO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 789 CO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 790 CO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 791 CO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 792 CO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 793 CO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 794 CO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 795 CO₂CH₃ 2,6-diF-phenyl 4-morpholino 796 CO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 797 CO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 798 CO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 799 CO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 800 CO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 801 CH₂OCH₃ phenyl 2-(aminosulfonyl)phenyl 802 CH₂OCH₃ phenyl 2-(methylaminosulfonyl)phenyl 803 CH₂OCH₃ phenyl 1-pyrrolidinocarbonyl 804 CH₂OCH₃ phenyl 2-(methylsulfonyl)phenyl 805 CH₂OCH₃ phenyl 4-morpholino 806 CH₂OCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 807 CH₂OCH₃ phenyl 4-morpholinocarbonyl 808 CH₂OCH₃ phenyl 2-methyl-1-imidazolyl 809 CH₂OCH₃ phenyl 5-methyl-1-imidazolyl 810 CH₂OCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 811 CH₂OCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 812 CH₂OCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 813 CH₂OCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 814 CH₂OCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 815 CH₂OCH₃ 2-pyridyl 4-morpholino 816 CH₂OCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 817 CH₂OCH₃ 2-pyridyl 4-morpholinocarbonyl 818 CH₂OCH₃ 2-pyridyl 2-methyl-1-imidazolyl 819 CH₂OCH₃ 2-pyridyl 5-methyl-1-imidazolyl 820 CH₂OCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 821 CH₂OCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 822 CH₂OCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 823 CH₂OCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 824 CH₂OCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 825 CH₂OCH₃ 3-pyridyl 4-morpholino 826 CH₂OCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 827 CH₂OCH₃ 3-pyridyl 4-morpholinocarbonyl 828 CH₂OCH₃ 3-pyridyl 2-methyl-1-imidazolyl 829 CH₂OCH₃ 3-pyridyl 5-methyl-1-imidazolyl 830 CH₂OCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 831 CH₂OCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 832 CH₂OCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 833 CH₂OCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 834 CH₂OCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 835 CH₂OCH₃ 2-pyrimidyl 4-morpholino 836 CH₂OCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 837 CH₂OCH₃ 2-pyrimidyl 4-morpholinocarbonyl 838 CH₂OCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 839 CH₂OCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 840 CH₂OCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 841 CH₂OCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 842 CH₂OCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 843 CH₂OCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 844 CH₂OCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 845 CH₂OCH₃ 5-pyrimidyl 4-morpholino 846 CH₂OCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 847 CH₂OCH₃ 5-pyrimidyl 4-morpholinocarbonyl 848 CH₂OCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 849 CH₂OCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 850 CH₂OCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 851 CH₂OCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 852 CH₂OCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 853 CH₂OCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 854 CH₂OCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 855 CH₂OCH₃ 2-Cl-phenyl 4-morpholino 856 CH₂OCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 857 CH₂OCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 858 CH₂OCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 859 CH₂OCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 860 CH₂OCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 861 CH₂OCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 862 CH₂OCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 863 CH₂OCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 864 CH₂OCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 865 CH₂OCH₃ 2-F-phenyl 4-morpholino 866 CH₂OCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 867 CH₂OCH₃ 2-F-phenyl 4-morpholinocarbonyl 868 CH₂OCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 869 CH₂OCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 870 CH₂OCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 871 CH₂OCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 872 CH₂OCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 873 CH₂OCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 874 CH₂OCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 875 CH₂OCH₃ 2,6-diF-phenyl 4-morpholino 876 CH₂OCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 877 CH₂OCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 878 CH₂OCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 879 CH₂OCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 880 CH₂OCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 881 CONH₂ phenyl 2-(aminosulfonyl)phenyl 882 CONH₂ phenyl 2-(methylaminosulfonyl)phenyl 883 CONH₂ phenyl 1-pyrrolidinocarbonyl 884 CONH₂ phenyl 2-(methylsulfonyl)phenyl 885 CONH₂ phenyl 4-morpholino 886 CONH₂ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 887 CONH₂ phenyl 4-morpholinocarbonyl 888 CONH₂ phenyl 2-methyl-1-imidazolyl 889 CONH₂ phenyl 5-methyl-1-imidazolyl 890 CONH₂ phenyl 2-methylsulfonyl-1-imidazolyl 891 CONH₂ 2-pyridyl 2-(aminosulfonyl)phenyl 892 CONH₂ 2-pyridyl 2-(methylaminosulfonyl)phenyl 893 CONH₂ 2-pyridyl 1-pyrrolidinocarbonyl 894 CONH₂ 2-pyridyl 2-(methylsulfonyl)phenyl 895 CONH₂ 2-pyridyl 4-morpholino 896 CONH₂ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 897 CONH₂ 2-pyridyl 4-morpholinocarbonyl 898 CONH₂ 2-pyridyl 2-methyl-1-imidazolyl 899 CONH₂ 2-pyridyl 5-methyl-1-imidazolyl 900 CONH₂ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 901 CONH₂ 3-pyridyl 2-(aminosulfonyl)phenyl 902 CONH₂ 3-pyridyl 2-(methylaminosulfonyl)phenyl 903 CONH₂ 3-pyridyl 1-pyrrolidinocarbonyl 904 CONH₂ 3-pyridyl 2-(methylsulfonyl)phenyl 905 CONH₂ 3-pyridyl 4-morpholino 906 CONH₂ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 907 CONH₂ 3-pyridyl 4-morpholinocarbonyl 908 CONH₂ 3-pyridyl 2-methyl-1-imidazolyl 909 CONH₂ 3-pyridyl 5-methyl-1-imidazolyl 910 CONH₂ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 911 CONH₂ 2-pyrimidyl 2-(aminosulfonyl)phenyl 912 CONH₂ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 913 CONH₂ 2-pyrimidyl 1-pyrrolidinocarbonyl 914 CONH₂ 2-pyrimidyl 2-(methylsulfonyl)phenyl 915 CONH₂ 2-pyrimidyl 4-morpholino 916 CONH₂ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 917 CONH₂ 2-pyrimidyl 4-morpholinocarbonyl 918 CONH₂ 2-pyrimidyl 2-methyl-1-imidazolyl 919 CONH₂ 2-pyrimidyl 5-methyl-1-imidazolyl 920 CONH₂ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 921 CONH₂ 5-pyrimidyl 2-(aminosulfonyl)phenyl 922 CONH₂ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 923 CONH₂ 5-pyrimidyl 1-pyrrolidinocarbonyl 924 CONH₂ 5-pyrimidyl 2-(methylsulfonyl)phenyl 925 CONH₂ 5-pyrimidyl 4-morpholino 926 CONH₂ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 927 CONH₂ 5-pyrimidyl 4-morpholinocarbonyl 928 CONH₂ 5-pyrimidyl 2-methyl-1-imidazolyl 929 CONH₂ 5-pyrimidyl 5-methyl-1-imidazolyl 930 CONH₂ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 931 CONH₂ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 932 CONH₂ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 933 CONH₂ 2-Cl-phenyl 1-pyrrolidinocarbonyl 934 CONH₂ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 935 CONH₂ 2-Cl-phenyl 4-morpholino 936 CONH₂ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 937 CONH₂ 2-Cl-phenyl 4-morpholinocarbonyl 938 CONH₂ 2-Cl-phenyl 2-methyl-1-imidazolyl 939 CONH₂ 2-Cl-phenyl 5-methyl-1-imidazolyl 940 CONH₂ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 941 CONH₂ 2-F-phenyl 2-(aminosulfonyl)phenyl 942 CONH₂ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 943 CONH₂ 2-F-phenyl 1-pyrrolidinocarbonyl 944 CONH₂ 2-F-phenyl 2-(methylsulfonyl)phenyl 945 CONH₂ 2-F-phenyl 4-morpholino 946 CONH₂ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 947 CONH₂ 2-F-phenyl 4-morpholinocarbonyl 948 CONH₂ 2-F-phenyl 2-methyl-1-imidazolyl 949 CONH₂ 2-F-phenyl 5-methyl-1-imidazolyl 950 CONH₂ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 951 CONH₂ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 952 CONH₂ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 953 CONH₂ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 954 CONH₂ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 955 CONH₂ 2,6-diF-phenyl 4-morpholino 956 CONH₂ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 957 CONH₂ 2,6-diF-phenyl 4-morpholinocarbonyl 958 CONH₂ 2,6-diF-phenyl 2-methyl-1-imidazolyl 959 CONH₂ 2,6-diF-phenyl 5-methyl-1-imidazolyl 960 CONH₂ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl

TABLE 5

For each example, DE is: (A) pyridin-4-yl-CH₂, (B) 2-amino-pyrimidin-4-yl, (C) 6-amino-pyridin-2-yl, (D) 3-amidino-4-F-phenyl, or (E) N-amidino-3-piperidinyl. Ex # A B  1 phenyl 2-(aminosulfonyl)phenyl  2 phenyl 2-(methylaminosulfonyl)phenyl  3 phenyl 1-pyrrolidinocarbonyl  4 phenyl 2-(methylsulfonyl)phenyl  5 phenyl 4-morpholino  6 phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  7 phenyl 4-morpholinocarbonyl  8 phenyl 2-methyl-1-imidazolyl  9 phenyl 5-methyl-1-imidazolyl 10 phenyl 2-methylsulfonyl-1-imidazolyl 11 2-pyridyl 2-(aminosulfonyl)phenyl 12 2-pyridyl 2-(methylaminosulfonyl)phenyl 13 2-pyridyl 1-pyrrolidinocarbonyl 14 2-pyridyl 2-(methylsulfonyl)phenyl 15 2-pyridyl 4-morpholino 16 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 17 2-pyridyl 4-morpholinocarbonyl 18 2-pyridyl 2-methyl-1-imidazolyl 19 2-pyridyl 5-methyl-1-imidazolyl 20 2-pyridyl 2-methylsulfonyl-1-imidazolyl 21 3-pyridyl 2-(aminosulfonyl)phenyl 22 3-pyridyl 2-(methylaminosulfonyl)phenyl 23 3-pyridyl 1-pyrrolidinocarbonyl 24 3-pyridyl 2-(methylsulfonyl)phenyl 25 3-pyridyl 4-morpholino 26 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 27 3-pyridyl 4-morpholinocarbonyl 28 3-pyridyl 2-methyl-1-imidazolyl 29 3-pyridyl 5-methyl-1-imidazolyl 30 3-pyridyl 2-methylsulfonyl-1-imidazolyl 31 2-pyrimidyl 2-(aminosulfonyl)phenyl 32 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 33 2-pyrimidyl 1-pyrrolidinocarbonyl 34 2-pyrimidyl 2-(methylsulfonyl)phenyl 35 2-pyrimidyl 4-morpholino 36 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 37 2-pyrimidyl 4-morpholinocarbonyl 38 2-pyrimidyl 2-methyl-1-imidazolyl 39 2-pyrimidyl 5-methyl-1-imidazolyl 40 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 41 5-pyrimidyl 2-(aminosulfonyl)phenyl 42 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 43 5-pyrimidyl 1-pyrrolidinocarbonyl 44 5-pyrimidyl 2-(methylsulfonyl)phenyl 45 5-pyrimidyl 4-morpholino 46 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 47 5-pyrimidyl 4-morpholinocarbonyl 48 5-pyrimidyl 2-methyl-1-imidazolyl 49 5-pyrimidyl 5-methyl-1-imidazolyl 50 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 51 2-Cl-phenyl 2-(aminosulfonyl)phenyl 52 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 53 2-Cl-phenyl 1-pyrrolidinocarbonyl 54 2-Cl-phenyl 2-(methylsulfonyl)phenyl 55 2-Cl-phenyl 4-morpholino 56 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 57 2-Cl-phenyl 4-morpholinocarbonyl 58 2-Cl-phenyl 2-methyl-1-imidazolyl 59 2-Cl-phenyl 5-methyl-1-imidazolyl 60 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 61 2-F-phenyl 2-(aminosulfonyl)phenyl 62 2-F-phenyl 2-(methylaminosulfonyl)phenyl 63 2-F-phenyl 1-pyrrolidinocarbonyl 64 2-F-phenyl 2-(methylsulfonyl)phenyl 65 2-F-phenyl 4-morpholino 66 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 67 2-F-phenyl 4-morpholinocarbonyl 68 2-F-phenyl 2-methyl-1-imidazolyl 69 2-F-phenyl 5-methyl-1-imidazolyl 70 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 71 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 72 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 73 2,6-diF-phenyl 1-pyrrolidinocarbonyl 74 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 75 2,6-diF-phenyl 4-morpholino 76 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 77 2,6-diF-phenyl 4-morpholinocarbonyl 78 2,6-diF-phenyl 2-methyl-1-imidazolyl 79 2,6-diF-phenyl 5-methyl-1-imidazolyl 80 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl

TABLE 6

Ex # R^(1a) A B  1 CH₃ phenyl 2-(aminosulfonyl)phenyl  2 CH₃ phenyl 2-(methylaminosulfonyl)phenyl  3 CH₃ phenyl 1-pyrrolidinocarbonyl  4 CH₃ phenyl 2-(methylsulfonyl)phenyl  5 CH₃ phenyl 4-morpholino  6 CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  7 CH₃ phenyl 4-morpholinocarbonyl  8 CH₃ phenyl 2-methyl-1-imidazolyl  9 CH₃ phenyl 5-methyl-1-imidazolyl  10 CH₃ phenyl 2-methylsulfonyl-1-imidazolyl  11 CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl  12 CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl  13 CH₃ 2-pyridyl 1-pyrrolidinocarbonyl  14 CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl  15 CH₃ 2-pyridyl 4-morpholino  16 CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  17 CH₃ 2-pyridyl 4-morpholinocarbonyl  18 CH₃ 2-pyridyl 2-methyl-1-imidazolyl  19 CH₃ 2-pyridyl 5-methyl-1-imidazolyl  20 CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl  21 CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl  22 CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl  23 CH₃ 3-pyridyl 1-pyrrolidinocarbonyl  24 CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl  25 CH₃ 3-pyridyl 4-morpholino  26 CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  27 CH₃ 3-pyridyl 4-morpholinocarbonyl  28 CH₃ 3-pyridyl 2-methyl-1-imidazolyl  29 CH₃ 3-pyridyl 5-methyl-1-imidazolyl  30 CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl  31 CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl  32 CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl  33 CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl  34 CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl  35 CH₃ 2-pyrimidyl 4-morpholino  36 CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  37 CH₃ 2-pyrimidyl 4-morpholinocarbonyl  38 CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl  39 CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl  40 CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl  41 CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl  42 CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl  43 CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl  44 CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl  45 CH₃ 5-pyrimidyl 4-morpholino  46 CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  47 CH₃ 5-pyrimidyl 4-morpholinocarbonyl  48 CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl  49 CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl  50 CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl  51 CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl  52 CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl  53 CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl  54 CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl  55 CH₃ 2-Cl-phenyl 4-morpholino  56 CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  57 CH₃ 2-Cl-phenyl 4-morpholinocarbonyl  58 CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl  59 CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl  60 CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl  61 CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl  62 CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl  63 CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl  64 CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl  65 CH₃ 2-F-phenyl 4-morpholino  66 CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  67 CH₃ 2-F-phenyl 4-morpholinocarbonyl  68 CH₃ 2-F-phenyl 2-methyl-1-imidazolyl  69 CH₃ 2-F-phenyl 5-methyl-1-imidazolyl  70 CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl  71 CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl  72 CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl  73 CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl  74 CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl  75 CH₃ 2,6-diF-phenyl 4-morpholino  76 CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  77 CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl  78 CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl  79 CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl  80 CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl  81 CH₂CH₃ phenyl 2-(aminosulfonyl)phenyl  82 CH₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl  83 CH₂CH₃ phenyl 1-pyrrolidinocarbonyl  84 CH₂CH₃ phenyl 2-(methylsulfonyl)phenyl  85 CH₂CH₃ phenyl 4-morpholino  86 CH₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  87 CH₂CH₃ phenyl 4-morpholinocarbonyl  88 CH₂CH₃ phenyl 2-methyl-1-imidazolyl  89 CH₂CH₃ phenyl 5-methyl-1-imidazolyl  90 CH₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl  91 CH₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl  92 CH₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl  93 CH₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl  94 CH₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl  95 CH₂CH₃ 2-pyridyl 4-morpholino  96 CH₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  97 CH₂CH₃ 2-pyridyl 4-morpholinocarbonyl  98 CH₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl  99 CH₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 100 CH₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 101 CH₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 102 CH₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 103 CH₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 104 CH₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 105 CH₂CH₃ 3-pyridyl 4-morpholino 106 CH₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 107 CH₂CH₃ 3-pyridyl 4-morpholinocarbonyl 108 CH₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 109 CH₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 110 CH₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 111 CH₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 112 CH₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 113 CH₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 114 CH₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 115 CH₂CH₃ 2-pyrimidyl 4-morpholino 116 CH₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 117 CH₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 118 CH₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 119 CH₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 120 CH₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 121 CH₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 122 CH₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 123 CH₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 124 CH₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 125 CH₂CH₃ 5-pyrimidyl 4-morpholino 126 CH₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 127 CH₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 128 CH₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 129 CH₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 130 CH₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 131 CH₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 132 CH₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 133 CH₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 134 CH₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 135 CH₂CH₃ 2-Cl-phenyl 4-morpholino 136 CH₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 137 CH₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 138 CH₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 139 CH₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 140 CH₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 141 CH₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 142 CH₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 143 CH₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 144 CH₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 145 CH₂CH₃ 2-F-phenyl 4-morpholino 146 CH₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 147 CH₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 148 CH₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 149 CH₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 150 CH₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 151 CH₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 152 CH₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 153 CH₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 154 CH₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 155 CH₂CH₃ 2,6-diF-phenyl 4-morpholino 156 CH₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 157 CH₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 158 CH₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 159 CH₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 160 CH₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 161 CF₃ phenyl 2-(aminosulfonyl)phenyl 162 CF₃ phenyl 2-(methylaminosulfonyl)phenyl 163 CF₃ phenyl 1-pyrrolidinocarbonyl 164 CF₃ phenyl 2-(methylsulfonyl)phenyl 165 CF₃ phenyl 4-morpholino 166 CF₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 167 CF₃ phenyl 4-morpholinocarbonyl 168 CF₃ phenyl 2-methyl-1-imidazolyl 169 CF₃ phenyl 5-methyl-1-imidazolyl 170 CF₃ phenyl 2-methylsulfonyl-1-imidazolyl 171 CF₃ 2-pyridyl 2-(aminosulfonyl)phenyl 172 CF₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 173 CF₃ 2-pyridyl 1-pyrrolidinocarbonyl 174 CF₃ 2-pyridyl 2-(methylsulfonyl)phenyl 175 CF₃ 2-pyridyl 4-morpholino 176 CF₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 177 CF₃ 2-pyridyl 4-morpholinocarbonyl 178 CF₃ 2-pyridyl 2-methyl-1-imidazolyl 179 CF₃ 2-pyridyl 5-methyl-1-imidazolyl 180 CF₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 181 CF₃ 3-pyridyl 2-(aminosulfonyl)phenyl 182 CF₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 183 CF₃ 3-pyridyl 1-pyrrolidinocarbonyl 184 CF₃ 3-pyridyl 2-(methylsulfonyl)phenyl 185 CF₃ 3-pyridyl 4-morpholino 186 CF₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 187 CF₃ 3-pyridyl 4-morpholinocarbonyl 188 CF₃ 3-pyridyl 2-methyl-1-imidazolyl 189 CF₃ 3-pyridyl 5-methyl-1-imidazolyl 190 CF₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 191 CF₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 192 CF₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 193 CF₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 194 CF₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 195 CF₃ 2-pyrimidyl 4-morpholino 196 CF₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 197 CF₃ 2-pyrimidyl 4-morpholinocarbonyl 198 CF₃ 2-pyrimidyl 2-methyl-1-imidazolyl 199 CF₃ 2-pyrimidyl 5-methyl-1-imidazolyl 200 CF₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 201 CF₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 202 CF₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 203 CF₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 204 CF₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 205 CF₃ 5-pyrimidyl 4-morpholino 206 CF₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 207 CF₃ 5-pyrimidyl 4-morpholinocarbonyl 208 CF₃ 5-pyrimidyl 2-methyl-1-imidazolyl 209 CF₃ 5-pyrimidyl 5-methyl-1-imidazolyl 210 CF₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 211 CF₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 212 CF₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 213 CF₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 214 CF₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 215 CF₃ 2-Cl-phenyl 4-morpholino 216 CF₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 217 CF₃ 2-Cl-phenyl 4-morpholinocarbonyl 218 CF₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 219 CF₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 220 CF₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 221 CF₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 222 CF₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 223 CF₃ 2-F-phenyl 1-pyrrolidinocarbonyl 224 CF₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 225 CF₃ 2-F-phenyl 4-morpholino 226 CF₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 227 CF₃ 2-F-phenyl 4-morpholinocarbonyl 228 CF₃ 2-F-phenyl 2-methyl-1-imidazolyl 229 CF₃ 2-F-phenyl 5-methyl-1-imidazolyl 230 CF₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 231 CF₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 232 CF₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 233 CF₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 234 CF₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 235 CF₃ 2,6-diF-phenyl 4-morpholino 236 CF₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 237 CF₃ 2,6-diF-phenyl 4-morpholinocarbonyl 238 CF₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 239 CF₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 240 CF₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 241 SCH₃ phenyl 2-(aminosulfonyl)phenyl 242 SCH₃ phenyl 2-(methylaminosulfonyl)phenyl 243 SCH₃ phenyl 1-pyrrolidinocarbonyl 244 SCH₃ phenyl 2-(methylsulfonyl)phenyl 245 SCH₃ phenyl 4-morpholino 246 SCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 247 SCH₃ phenyl 4-morpholinocarbonyl 248 SCH₃ phenyl 2-methyl-1-imidazolyl 249 SCH₃ phenyl 5-methyl-1-imidazolyl 250 SCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 251 SCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 252 SCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 253 SCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 254 SCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 255 SCH₃ 2-pyridyl 4-morpholino 256 SCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 257 SCH₃ 2-pyridyl 4-morpholinocarbonyl 258 SCH₃ 2-pyridyl 2-methyl-1-imidazolyl 259 SCH₃ 2-pyridyl 5-methyl-1-imidazolyl 260 SCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 261 SCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 262 SCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 263 SCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 264 SCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 265 SCH₃ 3-pyridyl 4-morpholino 266 SCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 267 SCH₃ 3-pyridyl 4-morpholinocarbonyl 268 SCH₃ 3-pyridyl 2-methyl-1-imidazolyl 269 SCH₃ 3-pyridyl 5-methyl-1-imidazolyl 270 SCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 271 SCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 272 SCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 273 SCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 274 SCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 275 SCH₃ 2-pyrimidyl 4-morpholino 276 SCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 277 SCH₃ 2-pyrimidyl 4-morpholinocarbonyl 278 SCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 279 SCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 280 SCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 281 SCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 282 SCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 283 SCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 284 SCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 285 SCH₃ 5-pyrimidyl 4-morpholino 286 SCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 287 SCH₃ 5-pyrimidyl 4-morpholinocarbonyl 288 SCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 289 SCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 290 SCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 291 SCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 292 SCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 293 SCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 294 SCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 295 SCH₃ 2-Cl-phenyl 4-morpholino 296 SCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 297 SCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 298 SCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 299 SCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 300 SCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 301 SCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 302 SCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 303 SCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 304 SCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 305 SCH₃ 2-F-phenyl 4-morpholino 306 SCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 307 SCH₃ 2-F-phenyl 4-morpholinocarbonyl 308 SCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 309 SCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 310 SCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 311 SCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 312 SCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 313 SCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 314 SCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 315 SCH₃ 2,6-diF-phenyl 4-morpholino 316 SCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 317 SCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 318 SCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 319 SCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 320 SCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 321 SOCH₃ phenyl 2-(aminosulfonyl)phenyl 322 SOCH₃ phenyl 2-(methylaminosulfonyl)phenyl 323 SOCH₃ phenyl 1-pyrrolidinocarbonyl 324 SOCH₃ phenyl 2-(methylsulfonyl)phenyl 325 SOCH₃ phenyl 4-morpholino 326 SOCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 327 SOCH₃ phenyl 4-morpholinocarbonyl 328 SOCH₃ phenyl 2-methyl-1-imidazolyl 329 SOCH₃ phenyl 5-methyl-1-imidazolyl 330 SOCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 331 SOCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 332 SOCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 333 SOCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 334 SOCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 335 SOCH₃ 2-pyridyl 4-morpholino 336 SOCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 337 SOCH₃ 2-pyridyl 4-morpholinocarbonyl 338 SOCH₃ 2-pyridyl 2-methyl-1-imidazolyl 339 SOCH₃ 2-pyridyl 5-methyl-1-imidazolyl 340 SOCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 341 SOCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 342 SOCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 343 SOCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 344 SOCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 345 SOCH₃ 3-pyridyl 4-morpholino 346 SOCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 347 SOCH₃ 3-pyridyl 4-morpholinocarbonyl 348 SOCH₃ 3-pyridyl 2-methyl-1-imidazolyl 349 SOCH₃ 3-pyridyl 5-methyl-1-imidazolyl 350 SOCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 351 SOCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 352 SOCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 353 SOCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 354 SOCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 355 SOCH₃ 2-pyrimidyl 4-morpholino 356 SOCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 357 SOCH₃ 2-pyrimidyl 4-morpholinocarbonyl 358 SOCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 359 SOCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 360 SOCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 361 SOCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 362 SOCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 363 SOCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 364 SOCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 365 SOCH₃ 5-pyrimidyl 4-morpholino 366 SOCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 367 SOCH₃ 5-pyrimidyl 4-morpholinocarbonyl 368 SOCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 369 SOCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 370 SOCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 371 SOCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 372 SOCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 373 SOCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 374 SOCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 375 SOCH₃ 2-Cl-phenyl 4-morpholino 376 SOCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 377 SOCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 378 SOCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 379 SOCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 380 SOCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 381 SOCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 382 SOCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 383 SOCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 384 SOCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 385 SOCH₃ 2-F-phenyl 4-morpholino 386 SOCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 387 SOCH₃ 2-F-phenyl 4-morpholinocarbonyl 388 SOCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 389 SOCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 390 SOCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 391 SOCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 392 SOCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 393 SOCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 394 SOCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 395 SOCH₃ 2,6-diF-phenyl 4-morpholino 396 SOCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 397 SOCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 398 SOCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 399 SOCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 400 SOCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 401 SO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 402 SO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 403 SO₂CH₃ phenyl 1-pyrrolidinocarbonyl 404 SO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 405 SO₂CH₃ phenyl 4-morpholino 406 SO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 407 SO₂CH₃ phenyl 4-morpholinocarbonyl 408 SO₂CH₃ phenyl 2-methyl-1-imidazolyl 409 SO₂CH₃ phenyl 5-methyl-1-imidazolyl 410 SO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 411 SO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 412 SO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 413 SO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 414 SO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 415 SO₂CH₃ 2-pyridyl 4-morpholino 416 SO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 417 SO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 418 SO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 419 SO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 420 SO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 421 SO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 422 SO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 423 SO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 424 SO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 425 SO₂CH₃ 3-pyridyl 4-morpholino 426 SO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 427 SO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 428 SO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 429 SO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 430 SO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 431 SO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 432 SO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 433 SO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 434 SO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 435 SO₂CH₃ 2-pyrimidyl 4-morpholino 436 SO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 437 SO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 438 SO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 439 SO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 440 SO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 441 SO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 442 SO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 443 SO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 444 SO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 445 SO₂CH₃ 5-pyrimidyl 4-morpholino 446 SO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 447 SO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 448 SO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 449 SO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 450 SO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 451 SO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 452 SO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 453 SO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 454 SO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 455 SO₂CH₃ 2-Cl-phenyl 4-morpholino 456 SO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 457 SO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 458 SO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 459 SO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 460 SO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-t-imidazolyl 461 SO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 462 SO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 463 SO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 464 SO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 465 SO₂CH₃ 2-F-phenyl 4-morpholino 466 SO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 467 SO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 468 SO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 469 SO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 470 SO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 471 SO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 472 SO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 473 SO₂CH₃ 2,6-diF-phenyl t-pyrrolidinocarbonyl 474 SO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 475 SO₂CH₃ 2,6-diF-phenyl 4-morpholino 476 SO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 477 SO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 478 SO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 479 SO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 480 SO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 481 CH₂NH— phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 482 CH₂NH— phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 483 CH₂NH— phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 484 CH₂NH— phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 485 CH₂NH— phenyl 4-morpholino SO₂CH₃ 486 CH₂NH— phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 487 CH₂NH— phenyl 4-morpholinocarbonyl SO₂CH₃ 488 CH₂NH— phenyl 2-methyl-1-imidazolyl SO₂CH₃ 489 CH₂NH— phenyl 5-methyl-1-imidazolyl SO₂CH₃ 490 CH₂NH— phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 491 CH₂NH— 2-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 492 CH₂NH— 2-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 493 CH₂NH— 2-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 494 CH₂NH— 2-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 495 CH₂NH— 2-pyridyl 4-morpholino SO₂CH₃ 496 CH₂NH— 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 497 CH₂NH— 2-pyridyl 4-morpholinocarbonyl SO₂CH₃ 498 CH₂NH— 2-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 499 CH₂NH— 2-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 500 CH₂NH— 2-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 501 CH₂NH— 3-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 502 CH₂NH— 3-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 503 CH₂NH— 3-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 504 CH₂NH— 3-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 505 CH₂NH— 3-pyridyl 4-morpholino SO₂CH₃ 506 CH₂NH— 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 507 CH₂NH— 3-pyridyl 4-morpholinocarbonyl SO₂CH₃ 508 CH₂NH— 3-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 509 CH₂NH— 3-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 510 CH₂NH— 3-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 511 CH₂NH— 2-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 512 CH₂NH— 2-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 513 CH₂NH— 2-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 514 CH₂NH— 2-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 515 CH₂NH— 2-pyrimidyl 4-morpholino SO₂CH₃ 516 CH₂NH— 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 517 CH₂NH— 2-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 518 CH₂NH— 2-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 519 CH₂NH— 2-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 520 CH₂NH— 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 521 CH₂NH— 5-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 522 CH₂NH— 5-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 523 CH₂NH— 5-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 524 CH₂NH— 5-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 525 CH₂NH— 5-pyrimidyl 4-morpholino SO₂CH₃ 526 CH₂NH— 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 527 CH₂NH— 5-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 528 CH₂NH— 5-Pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 529 CH₂NH— 5-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 530 CH₂NH— 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 531 CH₂NH— 2-Cl-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 532 CH₂NH— 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 533 CH₂NH— 2-Cl-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 534 CH₂NH— 2-Cl-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 535 CH₂NH— 2-Cl-phenyl 4-morpholino SO₂CH₃ 536 CH₂NH— 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 537 CH₂NH— 2-Cl-phenyl 4-morpholinocarbonyl SO₂CH₃ 538 CH₂NH— 2-Cl-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 539 CH₂NH— 2-Cl-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 540 CH₂NH— 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 541 CH₂NH— 2-F-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 542 CH₂NH— 2-F-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 543 CH₂NH— 2-F-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 544 CH₂NH— 2-F-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 545 CH₂NH— 2-F-phenyl 4-morpholino SO₂CH₃ 546 CH₂NH— 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 547 CH₂NH— 2-F-phenyl 4-morpholinocarbonyl SO₂CH₃ 548 CH₂NH— 2-F-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 549 CH₂NH— 2-F-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 550 CH₂NH— 2-F-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 551 CH₂NH— 2,6-diF-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 552 CH₂NH— 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 553 CH₂NH— 2,6-diF-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 554 CH₂NH— 2,6-diF-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 555 CH₂NH— 2,6-diF-phenyl 4-morpholino SO₂CH₃ 556 CH₂NH— 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 557 CH₂NH— 2,6-diF-phenyl 4-morpholinocarbonyl SO₂CH₃ 558 CH₂NH— 2,6-diF-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 559 CH₂NH— 2,6-diF-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 560 CH₂NH— 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 561 Cl phenyl 2-(aminosulfonyl)phenyl 562 Cl phenyl 2-(methylaminosulfonyl)phenyl 563 Cl phenyl 1-pyrrolidinocarbonyl 564 Cl phenyl 2-(methylsulfonyl)phenyl 565 Cl phenyl 4-morpholino 566 Cl phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 567 Cl phenyl 4-morpholinocarbonyl 568 Cl phenyl 2-methyl-1-imidazolyl 569 Cl phenyl 5-methyl-1-imidazolyl 570 Cl phenyl 2-methylsulfonyl-1-imidazolyl 571 Cl 2-pyridyl 2-(aminosulfonyl)phenyl 572 Cl 2-pyridyl 2-(methylaminosulfonyl)phenyl 573 Cl 2-pyridyl 1-pyrrolidinocarbonyl 574 Cl 2-pyridyl 2-(methylsulfonyl)phenyl 575 Cl 2-pyridyl 4-morpholino 576 Cl 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 577 Cl 2-pyridyl 4-morpholinocarbonyl 578 Cl 2-pyridyl 2-methyl-1-imidazolyl 579 Cl 2-pyridyl 5-methyl-1-imidazolyl 580 Cl 2-pyridyl 2-methylsulfonyl-1-imidazolyl 581 Cl 3-pyridyl 2-(aminosulfonyl)phenyl 582 Cl 3-pyridyl 2-(methylaminosulfonyl)phenyl 583 Cl 3-pyridyl 1-pyrrolidinocarbonyl 584 Cl 3-pyridyl 2-(methylsulfonyl)phenyl 585 Cl 3-pyridyl 4-morpholino 586 Cl 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 587 Cl 3-pyridyl 4-morpholinocarbonyl 588 Cl 3-pyridyl 2-methyl-1-imidazolyl 589 Cl 3-pyridyl 5-methyl-1-imidazolyl 590 Cl 3-pyridyl 2-methylsulfonyl-1-imidazolyl 591 Cl 2-pyrimidyl 2-(aminosulfonyl)phenyl 592 Cl 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 593 Cl 2-pyrimidyl 1-pyrrolidinocarbonyl 594 Cl 2-pyrimidyl 2-(methylsulfonyl)phenyl 595 Cl 2-pyrimidyl 4-morpholino 596 Cl 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 597 Cl 2-pyrimidyl 4-morpholinocarbonyl 598 Cl 2-pyrimidyl 2-methyl-1-imidazolyl 599 Cl 2-pyrimidyl 5-methyl-1-imidazolyl 600 Cl 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 601 Cl 5-pyrimidyl 2-(aminosulfonyl)phenyl 602 Cl 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 603 Cl 5-pyrimidyl 1-pyrrolidinocarbonyl 604 Cl 5-pyrimidyl 2-(methylsulfonyl)phenyl 605 Cl 5-pyrimidyl 4-morpholino 606 Cl 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 607 Cl 5-pyrimidyl 4-morpholinocarbonyl 608 Cl 5-pyrimidyl 2-methyl-1-imidazolyl 609 Cl 5-pyrimidyl 5-methyl-1-imidazolyl 610 Cl 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 611 Cl 2-Cl-phenyl 2-(aminosulfonyl)phenyl 612 Cl 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 613 Cl 2-Cl-phenyl 1-pyrrolidinocarbonyl 614 Cl 2-Cl-phenyl 2-(methylsulfonyl)phenyl 615 Cl 2-Cl-phenyl 4-morpholino 616 Cl 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 617 Cl 2-Cl-phenyl 4-morpholinocarbonyl 618 Cl 2-Cl-phenyl 2-methyl-1-imidazolyl 619 Cl 2-Cl-phenyl 5-methyl-1-imidazolyl 620 Cl 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 621 Cl 2-F-phenyl 2-(aminosulfonyl)phenyl 622 Cl 2-F-phenyl 2-(methylaminosulfonyl)phenyl 623 Cl 2-F-phenyl 1-pyrrolidinocarbonyl 624 Cl 2-F-phenyl 2-(methylsulfonyl)phenyl 625 Cl 2-F-phenyl 4-morpholino 626 Cl 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 627 Cl 2-F-phenyl 4-morpholinocarbonyl 628 Cl 2-F-phenyl 2-methyl-1-imidazolyl 629 Cl 2-F-phenyl 5-methyl-1-imidazolyl 630 Cl 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 631 Cl 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 632 Cl 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 633 Cl 2,6-diF-phenyl 1-pyrrolidinocarbonyl 634 Cl 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 635 Cl 2,6-diF-phenyl 4-morpholino 636 Cl 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 637 Cl 2,6-diF-phenyl 4-morpholinocarbonyl 638 Cl 2,6-diF-phenyl 2-methyl-1-imidazolyl 639 Cl 2,6-diF-phenyl 5-methyl-1-imidazolyl 640 Cl 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 641 F phenyl 2-(aminosulfonyl)phenyl 642 F phenyl 2-(methylaminosulfonyl)phenyl 643 F phenyl 1-pyrrolidinocarbonyl 644 F phenyl 2-(methylsulfonyl)phenyl 645 F phenyl 4-morpholino 646 F phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 647 F phenyl 4-morpholinocarbonyl 648 F phenyl 2-methyl-1-imidazolyl 649 F phenyl 5-methyl-1-imidazolyl 650 F phenyl 2-methylsulfonyl-1-imidazolyl 651 F 2-pyridyl 2-(aminosulfonyl)phenyl 652 F 2-pyridyl 2-(methylaminosulfonyl)phenyl 653 F 2-pyridyl 1-pyrrolidinocarbonyl 654 F 2-pyridyl 2-(methylsulfonyl)phenyl 655 F 2-pyridyl 4-morpholino 656 F 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 657 F 2-pyridyl 4-morpholinocarbonyl 658 F 2-pyridyl 2-methyl-1-imidazolyl 659 F 2-pyridyl 5-methyl-1-imidazolyl 660 F 2-pyridyl 2-methylsulfonyl-1-imidazolyl 661 F 3-pyridyl 2-(aminosulfonyl)phenyl 662 F 3-pyridyl 2-(methylaminosulfonyl)phenyl 663 F 3-pyridyl 1-pyrrolidinocarbonyl 664 F 3-pyridyl 2-(methylsulfonyl)phenyl 665 F 3-pyridyl 4-morpholino 666 F 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 667 F 3-pyridyl 4-morpholinocarbonyl 668 F 3-pyridyl 2-methyl-1-imidazolyl 669 F 3-pyridyl 5-methyl-1-imidazolyl 670 F 3-pyridyl 2-methylsulfonyl-1-imidazolyl 671 F 2-pyrimidyl 2-(aminosulfonyl)phenyl 672 F 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 673 F 2-pyrimidyl 1-pyrrolidinocarbonyl 674 F 2-pyrimidyl 2-(methylsulfonyl)phenyl 675 F 2-pyrimidyl 4-morpholino 676 F 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 677 F 2-pyrimidyl 4-morpholinocarbonyl 678 F 2-pyrimidyl 2-methyl-1-imidazolyl 679 F 2-pyrimidyl 5-methyl-1-imidazolyl 680 F 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 681 F 5-pyrimidyl 2-(aminosulfonyl)phenyl 682 F 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 683 F 5-pyrimidyl 1-pyrrolidinocarbonyl 684 F 5-pyrimidyl 2-(methylsulfonyl)phenyl 685 F 5-pyrimidyl 4-morpholino 686 F 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 687 F 5-pyrimidyl 4-morpholinocarbonyl 688 F 5-pyrimidyl 2-methyl-1-imidazolyl 689 F 5-pyrimidyl 5-methyl-1-imidazolyl 690 F 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 691 F 2-Cl-phenyl 2-(aminosulfonyl)phenyl 692 F 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 693 F 2-Cl-phenyl 1-pyrrolidinocarbonyl 694 F 2-Cl-phenyl 2-(methylsulfonyl)phenyl 695 F 2-Cl-phenyl 4-morpholino 696 F 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 697 F 2-Cl-phenyl 4-morpholinocarbonyl 698 F 2-Cl-phenyl 2-methyl-1-imidazolyl 699 F 2-Cl-phenyl 5-methyl-1-imidazolyl 700 F 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 701 F 2-F-phenyl 2-(aminosulfonyl)phenyl 702 F 2-F-phenyl 2-(methylaminosulfonyl)phenyl 703 F 2-F-phenyl 1-pyrrolidinocarbonyl 704 F 2-F-phenyl 2-(methylsulfonyl)phenyl 705 F 2-F-phenyl 4-morpholino 706 F 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 707 F 2-F-phenyl 4-morpholinocarbonyl 708 F 2-F-phenyl 2-methyl-1-imidazolyl 709 F 2-F-phenyl 5-methyl-1-imidazolyl 710 F 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 711 F 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 712 F 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 713 F 2,6-diF-phenyl 1-pyrrolidinocarbonyl 714 F 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 715 F 2,6-diF-phenyl 4-morpholino 716 F 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 717 F 2,6-diF-phenyl 4-morpholinocarbonyl 718 F 2,6-diF-phenyl 2-methyl-1-imidazolyl 719 F 2,6-diF-phenyl 5-methyl-1-imidazolyl 720 F 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 721 CO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 722 CO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 723 CO₂CH₃ phenyl 1-pyrrolidinocarbonyl 724 CO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 725 CO₂CH₃ phenyl 4-morpholino 726 CO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 727 CO₂CH₃ phenyl 4-morpholinocarbonyl 728 CO₂CH₃ phenyl 2-methyl-1-imidazolyl 729 CO₂CH₃ phenyl 5-methyl-1-imidazolyl 730 CO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 731 CO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 732 CO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 733 CO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 734 CO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 735 CO₂CH₃ 2-pyridyl 4-morpholino 736 CO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 737 CO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 738 CO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 739 CO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 740 CO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 741 CO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 742 CO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 743 CO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 744 CO₂CH₃ 3-pyridyl 2-(methylsulfonyl )phenyl 745 CO₂CH₃ 3-pyridyl 4-morpholino 746 CO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 747 CO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 748 CO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 749 CO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 750 CO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 751 CO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 752 CO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 753 CO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 754 CO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 755 CO₂CH₃ 2-pyrimidyl 4-morpholino 756 CO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 757 CO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 758 CO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 759 CO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 760 CO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 761 CO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 762 CO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 763 CO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 764 CO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 765 CO₂CH₃ 5-pyrimidyl 4-morpholino 766 CO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 767 CO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 768 CO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 769 CO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 770 CO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 771 CO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 772 CO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 773 CO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 774 CO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 775 CO₂CH₃ 2-Cl-phenyl 4-morpholino 776 CO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 777 CO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 778 CO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 779 CO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 780 CO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 781 CO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 782 CO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 783 CO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 784 CO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 785 CO₂CH₃ 2-F-phenyl 4-morpholino 786 CO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 787 CO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 788 CO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 789 CO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 790 CO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 791 CO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 792 CO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 793 CO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 794 CO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 795 CO₂CH₃ 2,6-diF-phenyl 4-morpholino 796 CO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 797 CO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 798 CO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 799 CO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 800 CO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 801 CH₂OCH₃ phenyl 2-(aminosulfonyl)phenyl 802 CH₂OCH₃ phenyl 2-(methylaminosulfonyl)phenyl 803 CH₂OCH₃ phenyl 1-pyrrolidinocarbonyl 804 CH₂OCH₃ phenyl 2-(methylsulfonyl)phenyl 805 CH₂OCH₃ phenyl 4-morpholino 806 CH₂OCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 807 CH₂OCH₃ phenyl 4-morpholinocarbonyl 808 CH₂OCH₃ phenyl 2-methyl-1-imidazolyl 809 CH₂OCH₃ phenyl 5-methyl-1-imidazolyl 810 CH₂OCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 811 CH₂OCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 812 CH₂OCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 813 CH₂OCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 814 CH₂OCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 815 CH₂OCH₃ 2-pyridyl 4-morpholino 816 CH₂OCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 817 CH₂OCH₃ 2-pyridyl 4-morpholinocarbonyl 818 CH₂OCH₃ 2-pyridyl 2-methyl-1-imidazolyl 819 CH₂OCH₃ 2-pyridyl 5-methyl-1-imidazolyl 820 CH₂OCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 821 CH₂OCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 822 CH₂OCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 823 CH₂OCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 824 CH₂OCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 825 CH₂OCH₃ 3-pyridyl 4-morpholino 826 CH₂OCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 827 CH₂OCH₃ 3-pyridyl 4-morpholinocarbonyl 828 CH₂OCH₃ 3-pyridyl 2-methyl-1-imidazolyl 829 CH₂OCH₃ 3-pyridyl 5-methyl-1-imidazolyl 830 CH₂OCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 831 CH₂OCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 832 CH₂OCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 833 CH₂OCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 834 CH₂OCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 835 CH₂OCH₃ 2-pyrimidyl 4-morpholino 836 CH₂OCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 837 CH₂OCH₃ 2-pyrimidyl 4-morpholinocarbonyl 838 CH₂OCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 839 CH₂OCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 840 CH₂OCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 841 CH₂OCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 842 CH₂OCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 843 CH₂OCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 844 CH₂OCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 845 CH₂OCH₃ 5-pyrimidyl 4-morpholino 846 CH₂OCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 847 CH₂OCH₃ 5-pyrimidyl 4-morpholinocarbonyl 848 CH₂OCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 849 CH₂OCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 850 CH₂OCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 851 CH₂OCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 852 CH₂OCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 853 CH₂OCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 854 CH₂OCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 855 CH₂OCH₃ 2-Cl-phenyl 4-morpholino 856 CH₂OCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 857 CH₂OCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 858 CH₂OCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 859 CH₂OCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 860 CH₂OCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 861 CH₂OCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 862 CH₂OCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 863 CH₂OCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 864 CH₂OCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 865 CH₂OCH₃ 2-F-phenyl 4-morpholino 866 CH₂OCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 867 CH₂OCH₃ 2-F-phenyl 4-morpholinocarbonyl 868 CH₂OCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 869 CH₂OCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 879 CH₂OCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 871 CH₂OCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 872 CH₂OCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 873 CH₂OCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 874 CH₂OCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 875 CH₂OCH₃ 2,6-diF-phenyl 4-morpholino 876 CH₂OCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 877 CH₂OCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 878 CH₂OCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 879 CH₂OCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 880 CH₂OCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 881 CONH₂ phenyl 2-(aminosulfonyl)phenyl 882 CONH₂ phenyl 2-(methylaminosulfonyl)phenyl 883 CONH₂ phenyl 1-pyrrolidinocarbonyl 884 CONH₂ phenyl 2-(methylsulfonyl)phenyl 885 CONH₂ phenyl 4-morpholino 886 CONH₂ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 887 CONH₂ phenyl 4-morpholinocarbonyl 888 CONH₂ phenyl 2-methyl-1-imidazolyl 889 CONH₂ phenyl 5-methyl-1-imidazolyl 890 CONH₂ phenyl 2-methylsulfonyl-1-imidazolyl 891 CONH₂ 2-pyridyl 2-(aminosulfonyl)phenyl 892 CONH₂ 2-pyridyl 2-(methylaminosulfonyl)phenyl 893 CONH₂ 2-pyridyl 1-pyrrolidinocarbonyl 894 CONH₂ 2-pyridyl 2-(methylsulfonyl)phenyl 895 CONH₂ 2-pyridyl 4-morpholino 896 CONH₂ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 897 CONH₂ 2-pyridyl 4-morpholinocarbonyl 898 CONH₂ 2-pyridyl 2-methyl-1-imidazolyl 899 CONH₂ 2-pyridyl 5-methyl-1-imidazolyl 900 CONH₂ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 901 CONH₂ 3-pyridyl 2-(aminosulfonyl)phenyl 902 CONH₂ 3-pyridyl 2-(methylaminosulfonyl)phenyl 903 CONH₂ 3-pyridyl 1-pyrrolidinocarbonyl 904 CONH₂ 3-pyridyl 2-(methylsulfonyl)phenyl 905 CONH₂ 3-pyridyl 4-morpholino 906 CONH₂ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 907 CONH₂ 3-pyridyl 4-morpholinocarbonyl 908 CONH₂ 3-pyridyl 2-methyl-1-imidazolyl 909 CONH₂ 3-pyridyl 5-methyl-1-imidazolyl 910 CONH₂ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 911 CONH₂ 2-pyrimidyl 2-(aminosulfonyl)phenyl 912 CONH₂ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 913 CONH₂ 2-pyrimidyl 1-pyrrolidinocarbonyl 914 CONH₂ 2-pyrimidyl 2-(methylsulfonyl)phenyl 915 CONH₂ 2-pyrimidyl 4-morpholino 916 CONH₂ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 917 CONH₂ 2-pyrimidyl 4-morpholinocarbonyl 918 CONH₂ 2-pyrimidyl 2-methyl-1-imidazolyl 919 CONH₂ 2-pyrimidyl 5-methyl-1-1-imidazolyl 920 CONH₂ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 921 CONH₂ 5-pyrimidyl 2-(aminosulfonyl)phenyl 922 CONH₂ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 923 CONH₂ 5-pyrimidyl 1-pyrrolidinocarbonyl 924 CONH₂ 5-pyrimidyl 2-(methylsulfonyl)phenyl 925 CONH₂ 5-pyrimidyl 4-morpholino 926 CONH₂ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 927 CONH₂ 5-pyrimidyl 4-morpholinocarbonyl 928 CONH₂ 5-pyrimidyl 2-methyl-1-imidazolyl 929 CONH₂ 5-pyrimidyl 5-methyl-1-imidazolyl 930 CONH₂ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 931 CONH₂ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 932 CONH₂ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 933 CONH₂ 2-Cl-phenyl 1-pyrrolidinocarbonyl 934 CONH₂ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 935 CONH₂ 2-Cl-phenyl 4-morpholino 936 CONH₂ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 937 CONH₂ 2-Cl-phenyl 4-morpholinocarbonyl 938 CONH₂ 2-Cl-phenyl 2-methyl-1-imidazolyl 939 CONH₂ 2-Cl-phenyl 5-methyl-1-imidazolyl 940 CONH₂ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 941 CONH₂ 2-F-phenyl 2-(aminosulfonyl)phenyl 942 CONH₂ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 943 CONH₂ 2-F-phenyl 1-pyrrolidinocarbonyl 944 CONH₂ 2-F-phenyl 2-(methylsulfonyl)phenyl 945 CONH₂ 2-F-phenyl 4-morpholino 946 CONH₂ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 947 CONH₂ 2-F-phenyl 4-morpholinocarbonyl 948 CONH₂ 2-F-phenyl 2-methyl-1-imidazolyl 949 CONH₂ 2-F-phenyl 5-methyl-1-imidazolyl 950 CONH₂ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 951 CONH₂ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 952 CONH₂ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 953 CONH₂ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 954 CONH₂ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 955 CONH₂ 2,6-diF-phenyl 4-morpholino 956 CONH₂ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 957 CONH₂ 2,6-diF-phenyl 4-morpholinocarbonyl 958 CONH₂ 2,6-diF-phenyl 2-methyl-1-imidazolyl 959 CONH₂ 2,6-diF-phenyl 5-methyl-1-imidazolyl 960 CONH₂ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl

TABLE 7

Ex # R^(1a) A B  1 CH₃ phenyl 2-(aminosulfonyl)phenyl  2 CH₃ phenyl 2-(methylaminosulfonyl)phenyl  3 CH₃ phenyl 1-pyrrolidinocarbonyl  4 CH₃ phenyl 2-(methylsulfonyl)phenyl  5 CH₃ phenyl 4-morpholino  6 CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  7 CH₃ phenyl 4-morpholinocarbonyl  8 CH₃ phenyl 2-methyl-1-imidazolyl  9 CH₃ phenyl 5-methyl-1-imidazolyl  10 CH₃ phenyl 2-methylsulfonyl-1-imidazolyl  11 CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl  12 CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl  13 CH₃ 2-pyridyl 1-pyrrolidinocarbonyl  14 CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl  15 CH₃ 2-pyridyl 4-morpholino  16 CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  17 CH₃ 2-pyridyl 4-morpholinocarbonyl  18 CH₃ 2-pyridyl 2-methyl-1-imidazolyl  19 CH₃ 2-pyridyl 5-methyl-1-imidazolyl  20 CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl  21 CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl  22 CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl  23 CH₃ 3-pyridyl 1-pyrrolidinocarbonyl  24 CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl  25 CH₃ 3-pyridyl 4-morpholino  26 CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  27 CH₃ 3-pyridyl 4-morpholinocarbonyl  28 CH₃ 3-pyridyl 2-methyl-1-imidazolyl  29 CH₃ 3-pyridyl 5-methyl-1-imidazolyl  30 CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl  31 CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl  32 CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl  33 CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl  34 CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl  35 CH₃ 2-pyrimidyl 4-morpholino  36 CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  37 CH₃ 2-pyrimidyl 4-morpholinocarbonyl  38 CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl  39 CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl  40 CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl  41 CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl  42 CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl  43 CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl  44 CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl  45 CH₃ 5-pyrimidyl 4-morpholino  46 CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  47 CH₃ 5-pyrimidyl 4-morpholinocarbonyl  48 CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl  49 CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl  50 CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl  51 CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl  52 CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl  53 CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl  54 CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl  55 CH₃ 2-Cl-phenyl 4-morpholino  56 CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  57 CH₃ 2-Cl-phenyl 4-morpholinocarbonyl  58 CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl  59 CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl  60 CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl  61 CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl  62 CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl  63 CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl  64 CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl  65 CH₃ 2-F-phenyl 4-morpholino  66 CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  67 CH₃ 2-F-phenyl 4-morpholinocarbonyl  68 CH₃ 2-F-phenyl 2-methyl-1-imidazolyl  69 CH₃ 2-F-phenyl 5-methyl-1-imidazolyl  70 CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl  71 CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl  72 CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl  73 CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl  74 CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl  75 CH₃ 2,6-diF-phenyl 4-morpholino  76 CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  77 CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl  78 CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl  79 CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl  80 CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl  81 CH₂CH₃ phenyl 2-(aminosulfonyl)phenyl  82 CH₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl  83 CH₂CH₃ phenyl 1-pyrrolidinocarbonyl  84 CH₂CH₃ phenyl 2-(methylsulfonyl)phenyl  85 CH₂CH₃ phenyl 4-morpholino  86 CH₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  87 CH₂CH₃ phenyl 4-morpholinocarbonyl  88 CH₂CH₃ phenyl 2-methyl-1-imidazolyl  89 CH₂CH₃ phenyl 5-methyl-1-imidazolyl  90 CH₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl  91 CH₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl  92 CH₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl  93 CH₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl  94 CH₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl  95 CH₂CH₃ 2-pyridyl 4-morpholino  96 CH₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl  97 CH₂CH₃ 2-pyridyl 4-morpholinocarbonyl  98 CH₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl  99 CH₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 100 CH₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 101 CH₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 102 CH₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 103 CH₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 104 CH₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 105 CH₂CH₃ 3-pyridyl 4-morpholino 106 CH₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 107 CH₂CH₃ 3-pyridyl 4-morpholinocarbonyl 108 CH₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 109 CH₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 110 CH₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 111 CH₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 112 CH₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 113 CH₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 114 CH₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 115 CH₂CH₃ 2-pyrimidyl 4-morpholino 116 CH₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 117 CH₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 118 CH₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 119 CH₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 120 CH₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 121 CH₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 122 CH₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 123 CH₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 124 CH₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 125 CH₂CH₃ 5-pyrimidyl 4-morpholino 126 CH₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 127 CH₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 128 CH₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 129 CH₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 130 CH₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 131 CH₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 132 CH₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 133 CH₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 134 CH₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 135 CH₂CH₃ 2-Cl-phenyl 4-morpholino 136 CH₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 137 CH₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 138 CH₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 139 CH₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 140 CH₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 141 CH₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 142 CH₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 143 CH₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 144 CH₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 145 CH₂CH₃ 2-F-phenyl 4-morpholino 146 CH₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 147 CH₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 148 CH₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 149 CH₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 150 CH₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 151 CH₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 152 CH₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 153 CH₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 154 CH₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 155 CH₂CH₃ 2,6-diF-phenyl 4-morpholino 156 CH₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 157 CH₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 158 CH₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 159 CH₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 160 CH₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 161 CF₃ phenyl 2-(aminosulfonyl)phenyl 162 CF₃ phenyl 2-(methylaminosulfonyl)phenyl 163 CF₃ phenyl 1-pyrrolidinocarbonyl 164 CF₃ phenyl 2-(methylsulfonyl)phenyl 165 CF₃ phenyl 4-morpholino 166 CF₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 167 CF₃ phenyl 4-morpholinocarbonyl 168 CF₃ phenyl 2-methyl-1-imidazolyl 169 CF₃ phenyl 5-methyl-1-imidazolyl 170 CF₃ phenyl 2-methylsulfonyl-1-imidazolyl 171 CF₃ 2-pyridyl 2-(aminosulfonyl)phenyl 172 CF₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 173 CF₃ 2-pyridyl 1-pyrrolidinocarbonyl 174 CF₃ 2-pyridyl 2-(methylsulfonyl)phenyl 175 CF₃ 2-pyridyl 4-morpholino 176 CF₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 177 CF₃ 2-pyridyl 4-morpholinocarbonyl 178 CF₃ 2-pyridyl 2-methyl-1-imidazolyl 179 CF₃ 2-pyridyl 5-methyl-1-imidazolyl 180 CF₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 181 CF₃ 3-pyridyl 2-(aminosulfonyl)phenyl 182 CF₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 183 CF₃ 3-pyridyl 1-pyrrolidinocarbonyl 184 CF₃ 3-pyridyl 2-(methylsulfonyl)phenyl 185 CF₃ 3-pyridyl 4-morpholino 186 CF₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 187 CF₃ 3-pyridyl 4-morpholinocarbonyl 188 CF₃ 3-pyridyl 2-methyl-1-imidazolyl 189 CF₃ 3-pyridyl 5-methyl-1-imidazolyl 190 CF₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 191 CF₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 192 CF₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 193 CF₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 194 CF₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 195 CF₃ 2-pyrimidyl 4-morpholino 196 CF₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 197 CF₃ 2-pyrimidyl 4-morpholinocarbonyl 198 CF₃ 2-pyrimidyl 2-methyl-1-imidazolyl 199 CF₃ 2-pyrimidyl 5-methyl-1-imidazolyl 200 CF₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 201 CF₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 202 CF₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 203 CF₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 204 CF₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 205 CF₃ 5-pyrimidyl 4-morpholino 206 CF₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 207 CF₃ 5-pyrimidyl 4-morpholinocarbonyl 208 CF₃ 5-pyrimidyl 2-methyl-1-imidazolyl 209 CF₃ 5-pyrimidyl 5-methyl-1-imidazolyl 210 CF₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 211 CF₃ 2-C1-phenyl 2-(aminosulfonyl)phenyl 212 CF₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 213 CF₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 214 CF₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 215 CF₃ 2-Cl-phenyl 4-morpholino 216 CF₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 217 CF₃ 2-Cl-phenyl 4-morpholinocarbonyl 218 CF₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 219 CF₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 220 CF₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 221 CF₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 222 CF₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 223 CF₃ 2-F-phenyl 1-pyrrolidinocarbonyl 224 CF₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 225 CF₃ 2-F-phenyl 4-morpholino 226 CF₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 227 CF₃ 2-F-phenyl 4-morpholinocarbonyl 228 CF₃ 2-F-phenyl 2-methyl-1-imidazolyl 229 CF₃ 2-F-phenyl 5-methyl-1-imidazolyl 230 CF₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 231 CF₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 232 CF₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 233 CF₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 234 CF₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 235 CF₃ 2,6-diF-phenyl 4-morpholino 236 CF₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 237 CF₃ 2,6-diF-phenyl 4-morpholinocarbonyl 238 CF₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 239 CF₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 240 CF₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 241 SCH₃ phenyl 2-(aminosulfonyl)phenyl 242 SCH₃ phenyl 2-(methylaminosulfonyl)phenyl 243 SCH₃ phenyl 1-pyrrolidinocarbonyl 244 SCH₃ phenyl 2-(methylsulfonyl)phenyl 245 SCH₃ phenyl 4-morpholino 246 SCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 247 SCH₃ phenyl 4-morpholinocarbonyl 248 SCH₃ phenyl 2-methyl-1-imidazolyl 249 SCH₃ phenyl 5-methyl-1-imidazolyl 250 SCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 251 SCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 252 SCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 253 SCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 254 SCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 255 SCH₃ 2-pyridyl 4-morpholino 256 SCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 257 SCH₃ 2-pyridyl 4-morpholinocarbonyl 258 SCH₃ 2-pyridyl 2-methyl-1-imidazolyl 259 SCH₃ 2-pyridyl 5-methyl-1-imidazolyl 260 SCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 261 SCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 262 SCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 263 SCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 264 SCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 265 SCH₃ 3-pyridyl 4-morpholino 266 SCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 267 SCH₃ 3-pyridyl 4-morpholinocarbonyl 268 SCH₃ 3-pyridyl 2-methyl-1-imidazolyl 269 SCH₃ 3-pyridyl 5-methyl-1-imidazolyl 270 SCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 271 SCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 272 SCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 273 SCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 274 SCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 275 SCH₃ 2-pyrimidyl 4-morpholino 276 SCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 277 SCH₃ 2-pyrimidyl 4-morpholinocarbonyl 278 SCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 279 SCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 280 SCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 281 SCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 282 SCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 283 SCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 284 SCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 285 SCH₃ 5-pyrimidyl 4-morpholino 286 SCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 287 SCH₃ 5-pyrimidyl 4-morpholinocarbonyl 288 SCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 289 SCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 290 SCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 291 SCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 292 SCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 293 SCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 294 SCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 295 SCH₃ 2-Cl-phenyl 4-morpholino 296 SCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 297 SCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 298 SCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 299 SCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 300 SCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 301 SCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 302 SCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 303 SCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 304 SCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 305 SCH₃ 2-F-phenyl 4-morpholino 306 SCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 307 SCH₃ 2-F-phenyl 4-morpholinocarbonyl 308 SCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 309 SCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 310 SCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 311 SCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 312 SCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 313 SCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 314 SCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 315 SCH₃ 2,6-diF-phenyl 4-morpholino 316 SCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 317 SCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 318 SCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 319 SCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 320 SCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 321 SOCH₃ phenyl 2-(aminosulfonyl)phenyl 322 SOCH₃ phenyl 2-(methylaminosulfonyl)phenyl 323 SOCH₃ phenyl 1-pyrrolidinocarbonyl 324 SOCH₃ phenyl 2-(methylsulfonyl)phenyl 325 SOCH₃ phenyl 4-morpholino 326 SOCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 327 SOCH₃ phenyl 4-morpholinocarbonyl 328 SOCH₃ phenyl 2-methyl-1-imidazolyl 329 SOCH₃ phenyl 5-methyl-1-imidazolyl 330 SOCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 331 SOCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 332 SOCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 333 SOCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 334 SOCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 335 SCCH₃ 2-pyridyl 4-morpholino 336 SOCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 337 SOCH₃ 2-pyridyl 4-morpholinocarbonyl 338 SOCH₃ 2-pyridyl 2-methyl-1-imidazolyl 339 SOCH₃ 2-pyridyl 5-methyl-1-imidazolyl 340 SOCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 341 SOCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 342 SOCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 343 SOCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 344 SOCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 345 SOCH₃ 3-pyridyl 4-morpholino 346 SOCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 347 SOCH₃ 3-pyridyl 4-morpholinocarbonyl 348 SOCH₃ 3-pyridyl 2-methyl-1-imidazolyl 349 SOCH₃ 3-pyridyl 5-methyl-1-imidazolyl 350 SOCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 351 SOCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 352 SOCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 353 SOCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 354 SOCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 355 SOCH₃ 2-pyrimidyl 4-morpholino 356 SOCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 357 SOCH₃ 2-pyrimidyl 4-morpholinocarbonyl 358 SOCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 359 SOCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 360 SOCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 361 SOCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 362 SOCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 363 SOCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 364 SOCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 365 SOCH₃ 5-pyrimidyl 4-morpholino 366 SOCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 367 SOCH₃ 5-pyrimidyl 4-morpholinocarbonyl 368 SOCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 369 SOCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 370 SOCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 371 SOCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 372 SOCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 373 SOCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 374 SOCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 375 SOCH₃ 2-Cl-phenyl 4-morpholino 376 SOCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 377 SOCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 378 SOCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 379 SOCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 380 SOCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 381 SOCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 382 SOCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 383 SOCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 384 SOCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 385 SOCH₃ 2-F-phenyl 4-morpholino 386 SOCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 387 SOCH₃ 2-F-phenyl 4-morpholinocarbonyl 388 SOCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 389 SOCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 390 SOCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 391 SOCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 392 SOCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 393 SOCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 394 SOCH₃ 2,6-diF-phenyl 2,-(methylsulfonyl)phenyl 395 SOCH₃ 2,6-diF-phenyl 4-morpholino 396 SOCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 397 SOCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 398 SOCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 399 SOCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 400 SOCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 401 SO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 402 SO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 403 SO₂CH₃ phenyl 1-pyrrolidinocarbonyl 404 SO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 405 SO₂CH₃ phenyl 4-morpholino 406 SO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 407 SO₂CH₃ phenyl 4-morpholinocarbonyl 408 SO₂CH₃ phenyl 2-methyl-1-imidazolyl 409 SO₂CH₃ phenyl 5-methyl-1-imidazolyl 410 SO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 411 SO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 412 SO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 413 SO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 414 SO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 415 SO₂CH₃ 2-pyridyl 4-morpholino 416 SO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 417 SO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 418 SO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 419 SO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 420 SO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 421 SO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 422 SO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 423 SO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 424 SO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 425 SO₂CH₃ 3-pyridyl 4-morpholino 426 SO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 427 SO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 428 SO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 429 SO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 430 SO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 431 SO₂CH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 432 SO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 433 SO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 434 SO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 435 SO₂CH₃ 2-pyrimidyl 4-morpholino 436 SO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 437 SO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 438 SO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 439 SO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 440 SO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 441 SO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 442 SO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 443 SO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 444 SO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 445 SO₂CH₃ 5-pyrimidyl 4-morpholino 446 SO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 447 SO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 448 SO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 449 SO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 450 SO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 451 SO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 452 SO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 453 SO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 454 SO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 455 SO₂CH₃ 2-Cl-phenyl 4-morpholino 456 SO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 457 SO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 458 SO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 459 SO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 460 SO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 461 SO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 462 SO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 463 SO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 464 SO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 465 SO₂CH₃ 2-F-phenyl 4-morpholino 466 SO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 467 SO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 468 SO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 469 SO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 470 SO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 471 SO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 472 SO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 473 SO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 474 SO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 475 SO₂CH₃ 2,6-diF-phenyl 4-morpholino 476 SO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 477 SO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 478 SO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 479 SO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 480 SO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 481 CH₂NH— phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 482 CH₂NH— phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 483 CH₂NH— phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 484 CH₂NH— phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 485 CH₂NH— phenyl 4-morpholino SO₂CH₃ 486 CH₂NH— phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 487 CH₂NH— phenyl 4-morpholinocarbonyl SO₂CH₃ 488 CH₂NH— phenyl 2-methyl-1-imidazolyl SO₂CH₃ 489 CH₂NH— phenyl 5-methyl-1-imidazolyl SO₂CH₃ 490 CH₂NH— phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 491 CH₂NH— 2-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 492 CH₂NH— 2-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 493 CH₂NH— 2-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 494 CH₂NH— 2-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 495 CH₂NH— 2-pyridyl 4-morpholino SO₂CH₃ 496 CH₂NH— 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 497 CH₂NH— 2-pyridyl 4-morpholinocarbonyl SO₂CH₃ 498 CH₂NH— 2-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 499 CH₂NH— 2-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 500 CH₂NH— 2-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 501 CH₂NH— 3-pyridyl 2-(aminosulfonyl)phenyl SO₂CH₃ 502 CH₂NH— 3-pyridyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 503 CH₂NH— 3-pyridyl 1-pyrrolidinocarbonyl SO₂CH₃ 504 CH₂NH— 3-pyridyl 2-(methylsulfonyl)phenyl SO₂CH₃ 505 CH₂NH— 3-pyridyl 4-morpholino SO₂CH₃ 506 CH₂NH— 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 507 CH₂NH— 3-pyridyl 4-morpholinocarbonyl SO₂CH₃ 508 CH₂NH— 3-pyridyl 2-methyl-1-imidazolyl SO₂CH₃ 509 CH₂NH— 3-pyridyl 5-methyl-1-imidazolyl SO₂CH₃ 510 CH₂NH— 3-pyridyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 511 CH₂NH— 2-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 512 CH₂NH— 2-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 513 CH₂NH— 2-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 514 CH₂NH— 2-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 515 CH₂NH— 2-pyrimidyl 4-morpholino SO₂CH₃ 516 CH₂NH— 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 517 CH₂NH— 2-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 518 CH₂NH— 2-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 519 CH₂NH— 2-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 520 CH₂NH— 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 521 CH₂NH— 5-pyrimidyl 2-(aminosulfonyl)phenyl SO₂CH₃ 522 CH₂NH— 5-pyrimidyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 523 CH₂NH— 5-pyrimidyl 1-pyrrolidinocarbonyl SO₂CH₃ 524 CH₂NH— 5-pyrimidyl 2-(methylsulfonyl)phenyl SO₂CH₃ 525 CH₂NH— 5-pyrimidyl 4-morpholino SO₂CH₃ 526 CH₂NH— 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 527 CH₂NH— 5-pyrimidyl 4-morpholinocarbonyl SO₂CH₃ 528 CH₂NH— 5-pyrimidyl 2-methyl-1-imidazolyl SO₂CH₃ 529 CH₂NH— 5-pyrimidyl 5-methyl-1-imidazolyl SO₂CH₃ 530 CH₂NH— 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 531 CH₂NH— 2-Cl-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 532 CH₂NH— 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 533 CH₂NH— 2-Cl-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 534 CH₂NH— 2-Cl-phenyl 2-(methylsulfonyl)phenyl SO_(2‘CH) ₃ 535 CH₂NH— 2-Cl-phenyl 4-morpholino SO₂CH₃ 536 CH₂NH— 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 537 CH₂NH— 2-Cl-phenyl 4-morpholinocarbonyl SO₂CH₃ 538 CH₂NH— 2-Cl-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 539 CH₂NH— 2-Cl-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 540 CH₂NH— 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 541 CH₂NH— 2-F-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 542 CH₂NH— 2-F-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 543 CH₂NH— 2-F-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 544 CH₂NH— 2-F-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 545 CH₂NH— 2-F-phenyl 4-morpholino SO₂CH₃ 546 CH₂NH— 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 547 CH₂NH— 2-F-phenyl 4-morpholinocarbonyl SO₂CH₃ 548 CH₂NH— 2-F-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 549 CH₂NH— 2-F-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 550 CH₂NH— 2-F-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 551 CH₂NH— 2,6-diF-phenyl 2-(aminosulfonyl)phenyl SO₂CH₃ 552 CH₂NH— 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl SO₂CH₃ 553 CH₂NH— 2,6-diF-phenyl 1-pyrrolidinocarbonyl SO₂CH₃ 554 CH₂NH— 2,6-diF-phenyl 2-(methylsulfonyl)phenyl SO₂CH₃ 555 CH₂NH— 2,6-diF-phenyl 4-morpholino SO₂CH₃ 556 CH₂NH— 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl SO₂CH₃ 557 CH₂NH— 2,6-diF-phenyl 4-morpholinocarbonyl SO₂CH₃ 558 CH₂NH— 2,6-diF-phenyl 2-methyl-1-imidazolyl SO₂CH₃ 559 CH₂NH— 2,6-diF-phenyl 5-methyl-1-imidazolyl SO₂CH₃ 560 CH₂NH— 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl SO₂CH₃ 561 Cl phenyl 2-(aminosulfonyl)phenyl 562 Cl phenyl 2-(methylaminosulfonyl)phenyl 563 Cl phenyl 1-pyrrolidinocarbonyl 564 Cl phenyl 2-(methylsulfonyl)phenyl 565 Cl phenyl 4-morpholino 566 Cl phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 567 Cl phenyl 4-morpholinocarbonyl 568 Cl phenyl 2-methyl-1-imidazolyl 569 Cl phenyl 5-methyl-1-imidazolyl 570 Cl phenyl 2-methylsulfonyl-1-imidazolyl 571 Cl 2-pyridyl 2-(aminosulfonyl)phenyl 572 Cl 2-pyridyl 2-(methylaminosulfonyl)phenyl 573 Cl 2-pyridyl 1-pyrrolidinocarbonyl 574 Cl 2-pyridyl 2-(methylsulfonyl)phenyl 575 Cl 2-pyridyl 4-morpholino 576 Cl 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 577 Cl 2-pyridyl 4-morpholinocarbonyl 578 Cl 2-pyridyl 2-methyl-l-imidazolyl 579 Cl 2-pyridyl 5-methyl-1-imidazolyl 580 Cl 2-pyridyl 2-methylsulfonyl-l-imidazolyl 581 Cl 3-pyridyl 2-(aminosulfonyl)phenyl 582 Cl 3-pyridyl 2-(methylaminosulfonyl)phenyl 583 Cl 3-pyridyl 1-pyrrolidinocarbonyl 584 Cl 3-pyridyl 2-(methylsulfonyl)phenyl 585 Cl 3-pyridyl 4-morpholino 586 Cl 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 587 Cl 3-pyridyl 4-morpholinocarbonyl 588 Cl 3-pyridyl 2-methyl-1-imidazolyl 589 Cl 3-pyridyl 5-methyl-1-imidazolyl 590 Cl 3-pyridyl 2-methylsulfonyl-1-imidazolyl 591 Cl 2-pyrimidyl 2-(aminosulfonyl)phenyl 592 Cl 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 593 Cl 2-pyrimidyl 1-pyrrolidinocarbonyl 594 Cl 2-pyrimidyl 2-(methylsulfonyl)phenyl 595 Cl 2-pyrimidyl 4-morpholino 596 Cl 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 597 Cl 2-pyrimidyl 4-morpholinocarbonyl 598 Cl 2-pyrimidyl 2-methyl-l-imidazolyl 599 Cl 2-pyrimidyl 5-methyl-l-imidazolyl 600 Cl 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 601 Cl 5-pyrimidyl 2-(aminosulfonyl)phenyl 602 Cl 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 603 Cl 5-pyrimidyl 1-pyrrolidinocarbonyl 604 Cl 5-pyrimidyl 2-(methylsulfonyl)phenyl 605 Cl 5-pyrimidyl 4-morpholino 606 Cl 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 607 Cl 5-pyrimidyl 4-morpholinocarbonyl 608 Cl 5-pyrimidyl 2-methyl-1-imidazolyl 609 Cl 5-pyrimidyl 5-methyl-1-imidazolyl 610 Cl 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 611 Cl 2-Cl-phenyl 2-(aminosulfonyl)phenyl 612 Cl 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 613 Cl 2-Cl-phenyl 1-pyrrolidinocarbonyl 614 Cl 2-Cl-phenyl 2-(methylsulfonyl)phenyl 615 Cl 2-Cl-phenyl 4-morpholino 616 Cl 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 617 Cl 2-Cl-phenyl 4-morpholinocarbonyl 618 Cl 2-Cl-phenyl 2-methyl-1-imidazolyl 619 Cl 2-Cl-phenyl 5-methyl-1-imidazolyl 620 Cl 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 621 Cl 2-F-phenyl 2-(aminosulfonyl)phenyl 622 Cl 2-F-phenyl 2-(methylaminosulfonyl)phenyl 623 Cl 2-F-phenyl 1-pyrrolidinocarbonyl 624 Cl 2-F-phenyl 2-(methylsulfonyl)phenyl 625 Cl 2-F-phenyl 4-morpholino 626 Cl 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 627 Cl 2-F-phenyl 4-morpholinocarbonyl 628 Cl 2-F-phenyl 2-methyl-1-imidazolyl 629 Cl 2-F-phenyl 5-methyl-1-imidazolyl 630 Cl 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 631 Cl 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 632 Cl 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 633 Cl 2,6-diF-phenyl 1-pyrrolidinocarbonyl 634 Cl 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 635 Cl 2,6-diF-phenyl 4-morpholino 636 Cl 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 637 Cl 2,6-diF-phenyl 4-morpholinocarbonyl 638 Cl 2,6-diF-phenyl 2-methyl-1-imidazolyl 639 Cl 2,6-diF-phenyl 5-methyl-1-imidazolyl 640 Cl 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 641 F phenyl 2-(aminosulfonyl)phenyl 642 F phenyl 2-(methylaminosulfonyl)phenyl 643 F phenyl 1-pyrrolidinocarbonyl 644 F phenyl 2-(methylsulfonyl)phenyl 645 F phenyl 4-morpholino 646 F phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 647 F phenyl 4-morpholinocarbonyl 648 F phenyl 2-methyl-1-imidazolyl 649 F phenyl 5-methyl-1-imidazolyl 650 F phenyl 2-methylsulfonyl-1-imidazolyl 651 F 2-pyridyl 2-(aminosulfonyl)phenyl 652 F 2-pyridyl 2-(methylaminosulfonyl)phenyl 653 F 2-pyridyl 1-pyrrolidinocarbonyl 654 F 2-pyridyl 2-(methylsulfonyl)phenyl 655 F 2-pyridyl 4-morpholinp 656 F 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 657 F 2-pyridyl 4-morpholinocarbonyl 658 F 2-pyridyl 2-methyl-1-imidazolyl 659 F 2-pyridyl 5-methyl-1-imidazolyl 660 F 2-pyridyl 2-methylsulfonyl-1-imidazolyl 661 F 3-pyridyl 2-(aminosulfonyl)phenyl 662 F 3-pyridyl 2-(methylaminosulfonyl)phenyl 663 F 3-pyridyl 1-pyrrolidinocarbonyl 664 F 3-pyridyl 2-(methylsulfonyl)phenyl 665 F 3-pyridyl 4-morpholino 666 F 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 667 F 3-pyridyl 4-morpholinocarbonyl 668 F 3-pyridyl 2-methyl-1-imidazolyl 669 F 3-pyridyl 5-methyl-1-imidazolyl 670 F 3-pyridyl 2-methylsulfonyl-1-imidazolyl 671 F 2-pyrimidyl 2-(aminosulfonyl)phenyl 672 F 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 673 F 2-pyrimidyl 1-pyrrolidinocarbonyl 674 F 2-pyrimidyl 2-(methylsulfonyl)phenyl 675 F 2-pyrimidyl 4-morpholino 676 F 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 677 F 2-pyrimidyl 4-morpholinocarbonyl 678 F 2-pyrimidyl 2-methyl-1-imidazolyl 679 F 2-pyrimidyl 5-methyl-1-imidazolyl 680 F 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 681 F 5-pyrimidyl 2-(aminosulfonyl)phenyl 682 F 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 683 F 5-pyrimidyl 1-pyrrolidinocarbonyl 684 F 5-pyrimidyl 2-(methylsulfonyl)phenyl 685 F 5-pyrimidyl 4-morpholino 686 F 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 687 F 5-pyrimidyl 4-morpholinocarbonyl 688 F 5-pyrimidyl 2-methyl-1-imidazolyl 689 F 5-pyrimidyl 5-methyl-1-imidazolyl 690 F 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 691 F 2-Cl-phenyl 2-(aminosulfonyl)phenyl 692 F 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 693 F 2-Cl-phenyl 1-pyrrolidinocarbonyl 694 F 2-Cl-phenyl 2-(methylsulfonyl)phenyl 695 F 2-Cl-phenyl 4-morpholino 696 F 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 697 F 2-Cl-phenyl 4-morpholinocarbonyl 698 F 2-Cl-phenyl 2-methyl-1-imidazolyl 699 F 2-Cl-phenyl 5-methyl-1-imidazolyl 700 F 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 701 F 2-F-phenyl 2-(aminosulfonyl)phenyl 702 F 2-F-phenyl 2-(methylaminosulfonyl)phenyl 703 F 2-F-phenyl 1-pyrrolidinocarbonyl 704 F 2-F-phenyl 2-(methylsulfonyl)phenyl 705 F 2-F-phenyl 4-morpholino 706 F 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 707 F 2-F-phenyl 4-morpholinocarbonyl 708 F 2-F-phenyl 2-methyl-1-imidazolyl 709 F 2-F-phenyl 5-methyl-i-imidazolyl 710 F 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 711 F 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 712 F 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 713 F 2,6-diF-phenyl 1-pyrrolidinocarbonyl 714 F 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 715 F 2,6-diF-phenyl 4-morpholino 716 F 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 717 F 2,6-diF-phenyl 4-morpholinocarbonyl 718 F 2,6-diF-phenyl 2-methyl-1-imidazolyl 719 F 2,6-diF-phenyl 5-methyl-1-imidazolyl 720 F 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 721 CO₂CH₃ phenyl 2-(aminosulfonyl)phenyl 722 CO₂CH₃ phenyl 2-(methylaminosulfonyl)phenyl 723 CO₂CH₃ phenyl 1-pyrrolidinocarbonyl 724 CO₂CH₃ phenyl 2-(methylsulfonyl)phenyl 725 CO₂CH₃ phenyl 4-morpholino 726 CO₂CH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 727 CO₂CH₃ phenyl 4-morpholinocarbonyl 728 CO₂CH₃ phenyl 2-methyl-1-imidazolyl 729 CO₂CH₃ phenyl 5-methyl-1-imidazolyl 730 CO₂CH₃ phenyl 2-methylsulfonyl-1-imidazolyl 731 CO₂CH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 732 CO₂CH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 733 CO₂CH₃ 2-pyridyl 1-pyrrolidinocarbonyl 734 CO₂CH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 735 CO₂CH₃ 2-pyridyl 4-morpholino 736 CO₂CH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 737 CO₂CH₃ 2-pyridyl 4-morpholinocarbonyl 738 CO₂CH₃ 2-pyridyl 2-methyl-1-imidazolyl 739 CO₂CH₃ 2-pyridyl 5-methyl-1-imidazolyl 740 CO₂CH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 741 CO₂CH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 742 CO₂CH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 743 CO₂CH₃ 3-pyridyl 1-pyrrolidinocarbonyl 744 CO₂CH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 745 CO₂CH₃ 3-pyridyl 4-morpholino 746 CO₂CH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 747 CO₂CH₃ 3-pyridyl 4-morpholinocarbonyl 748 CO₂CH₃ 3-pyridyl 2-methyl-1-imidazolyl 749 CO₂CH₃ 3-pyridyl 5-methyl-1-imidazolyl 750 CO₂CH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 751 CO₂CH₃ 2-pyrimiayl 2-(aminosulfonyl)phenyl 752 CO₂CH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 753 CO₂CH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 754 CO₂CH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 755 CO₂CH₃ 2-pyrimidyl 4-morpholino 756 CO₂CH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 757 CO₂CH₃ 2-pyrimidyl 4-morpholinocarbonyl 758 CO₂CH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 759 CO₂CH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 760 CO₂CH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 761 CO₂CH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 762 CO₂CH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 763 CO₂CH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 764 CO₂CH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 765 CO₂CH₃ 5-pyrimidyl 4-morpholino 766 CO₂CH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 767 CO₂CH₃ 5-pyrimidyl 4-morpholinocarbonyl 768 CO₂CH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 769 CO₂CH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 770 CO₂CH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 771 CO₂CH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 772 CO₂CH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 773 CO₂CH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 774 CO₂CH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 775 CO₂CH₃ 2-Cl-phenyl 4-morpholino 776 CO₂CH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 777 CO₂CH₃ 2-Cl-phenyl 4-morpholinocarbonyl 778 CO₂CH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 779 CO₂CH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 780 CO₂CH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 781 CO₂CH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 782 CO₂CH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 783 CO₂CH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 784 CO₂CH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 785 CO₂CH₃ 2-F-phenyl 4-morpholino 786 CO₂CH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 787 CO₂CH₃ 2-F-phenyl 4-morpholinocarbonyl 788 CO₂CH₃ 2-F-phenyl 2-methyl-1-imidazolyl 789 CO₂CH₃ 2-F-phenyl 5-methyl-1-imidazolyl 790 CO₂CH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 791 CO₂CH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 792 CO₂CH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 793 CO₂CH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 794 CO₂CH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 795 CO₂CH₃ 2,6-diF-phenyl 4-morpholino 796 CO₂CH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 797 CO₂CH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 798 CO₂CH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 799 CO₂CH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 800 CO₂CH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 801 CH₂OCH₃ phenyl 2-(aminosulfonyl)phenyl 802 CH₂OCH₃ phenyl 2-(methylaminosulfonyl)phenyl 803 CH₂OCH₃ phenyl 1-pyrrolidinocarbonyl 804 CH₂OCH₃ phenyl 2-(methylsulfonyl)phenyl 805 CH₂OCH₃ phenyl 4-morpholino 806 CH₂OCH₃ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 807 CH₂OCH₃ phenyl 4-morpholinocarbonyl 808 CH₂OCH₃ phenyl 2-methyl-1-imidazolyl 809 CH₂OCH₃ phenyl 5-methyl-1-imidazolyl 810 CH₂OCH₃ phenyl 2-methylsulfonyl-1-imidazolyl 811 CH₂OCH₃ 2-pyridyl 2-(aminosulfonyl)phenyl 812 CH₂OCH₃ 2-pyridyl 2-(methylaminosulfonyl)phenyl 813 CH₂OCH₃ 2-pyridyl 1-pyrrolidinocarbonyl 814 CH₂OCH₃ 2-pyridyl 2-(methylsulfonyl)phenyl 815 CH₂OCH₃ 2-pyridyl 4-morpholino 816 CH₂OCH₃ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 817 CH₂OCH₃ 2-pyridyl 4-morpholinocarbonyl 818 CH₂OCH₃ 2-pyridyl 2-methyl-1-imidazolyl 819 CH₂OCH₃ 2-pyridyl 5-methyl-1-imidazolyl 820 CH₂OCH₃ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 821 CH₂OCH₃ 3-pyridyl 2-(aminosulfonyl)phenyl 822 CH₂OCH₃ 3-pyridyl 2-(methylaminosulfonyl)phenyl 823 CH₂OCH₃ 3-pyridyl 1-pyrrolidinocarbonyl 824 CH₂OCH₃ 3-pyridyl 2-(methylsulfonyl)phenyl 825 CH₂OCH₃ 3-pyridyl 4-morpholino 826 CH₂OCH₃ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 827 CH₂OCH₃ 3-pyridyl 4-morpholinocarbonyl 828 CH₂OCH₃ 3-pyridyl 2-methyl-1-imidazolyl 829 CH₂OCH₃ 3-pyridyl 5-methyl-1-imidazolyl 830 CH₂OCH₃ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 831 CH₂OCH₃ 2-pyrimidyl 2-(aminosulfonyl)phenyl 832 CH₂OCH₃ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 833 CH₂OCH₃ 2-pyrimidyl 1-pyrrolidinocarbonyl 834 CH₂OCH₃ 2-pyrimidyl 2-(methylsulfonyl)phenyl 835 CH₂OCH₃ 2-pyrimidyl 4-morpholino 836 CH₂OCH₃ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 837 CH₂OCH₃ 2-pyrimidyl 4-morpholinocarbonyl 838 CH₂OCH₃ 2-pyrimidyl 2-methyl-1-imidazolyl 839 CH₂OCH₃ 2-pyrimidyl 5-methyl-1-imidazolyl 840 CH₂OCH₃ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 841 CH₂OCH₃ 5-pyrimidyl 2-(aminosulfonyl)phenyl 842 CH₂OCH₃ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 843 CH₂OCH₃ 5-pyrimidyl 1-pyrrolidinocarbonyl 844 CH₂OCH₃ 5-pyrimidyl 2-(methylsulfonyl)phenyl 845 CH₂OCH₃ 5-pyrimidyl 4-morpholino 846 CH₂OCH₃ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 847 CH₂OCH₃ 5-pyrimidyl 4-morpholinocarbonyl 848 CH₂OCH₃ 5-pyrimidyl 2-methyl-1-imidazolyl 849 CH₂OCH₃ 5-pyrimidyl 5-methyl-1-imidazolyl 850 CH₂OCH₃ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 851 CH₂OCH₃ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 852 CH₂OCH₃ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 853 CH₂OCH₃ 2-Cl-phenyl 1-pyrrolidinocarbonyl 854 CH₂OCH₃ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 855 CH₂OCH₃ 2-Cl-phenyl 4-morpholino 856 CH₂OCH₃ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 857 CH₂OCH₃ 2-Cl-phenyl 4-morpholinocarbonyl 858 CH₂OCH₃ 2-Cl-phenyl 2-methyl-1-imidazolyl 859 CH₂OCH₃ 2-Cl-phenyl 5-methyl-1-imidazolyl 860 CH₂OCH₃ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 861 CH₂OCH₃ 2-F-phenyl 2-(aminosulfonyl)phenyl 862 CH₂OCH₃ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 863 CH₂OCH₃ 2-F-phenyl 1-pyrrolidinocarbonyl 864 CH₂OCH₃ 2-F-phenyl 2-(methylsulfonyl)phenyl 865 CH₂OCH₃ 2-F-phenyl 4-morpholino 866 CH₂OCH₃ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 867 CH₂OCH₃ 2-F-phenyl 4-morpholinocarbonyl 868 CH₂OCH₃ 2-F-phenyl 2-methyl-1-imidazolyl 869 CH₂OCH₃ 2-F-phenyl 5-methyl-1-imidazolyl 870 CH₂OCH₃ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 871 CH₂OCH₃ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 872 CH₂OCH₃ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 873 CH₂OCH₃ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 874 CH₂OCH₃ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 875 CH₂OCH₃ 2,6-diF-phenyl 4-morpholino 876 CH₂OCH₃ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 877 CH₂OCH₃ 2,6-diF-phenyl 4-morpholinocarbonyl 878 CH₂OCH₃ 2,6-diF-phenyl 2-methyl-1-imidazolyl 879 CH₂OCH₃ 2,6-diF-phenyl 5-methyl-1-imidazolyl 880 CH₂OCH₃ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl 881 CONH₂ phenyl 2-(aminosulfonyl)phenyl 882 CONH₂ phenyl 2-(methylaminosulfonyl)phenyl 883 CONH₂ phenyl 1-pyrrolidinocarbonyl 884 CONH₂ phenyl 2-(methylsulfonyl)phenyl 885 CONH₂ phenyl 4-morpholino 886 CONH₂ phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 887 CONH₂ phenyl 4-morpholinocarbonyl 888 CONH₂ phenyl 2-methyl-1-imidazolyl 889 CONH₂ phenyl 5-methyl-1-imidazolyl 890 CONH₂ phenyl 2-methylsulfonyl-1-imidazolyl 891 CONH₂ 2-pyridyl 2-(aminosulfonyl)phenyl 892 CONH₂ 2-pyridyl 2-(methylaminosulfonyl)phenyl 893 CONH₂ 2-pyridyl 1-pyrrolidinocarbonyl 894 CONH₂ 2-pyridyl 2-(methylsulfonyl)phenyl 895 CONH₂ 2-pyridyl 4-morpholino 896 CONH₂ 2-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 897 CONH₂ 2-pyridyl 4-morpholinocarbonyl 898 CONH₂ 2-pyridyl 2-methyl-1-imidazolyl 899 CONH₂ 2-pyridyl 5-methyl-1-imidazolyl 900 CONH₂ 2-pyridyl 2-methylsulfonyl-1-imidazolyl 901 CONH₂ 3-pyridyl 2-(aminosulfonyl)phenyl 902 CONH₂ 3-pyridyl 2-(methylaminosulfonyl)phenyl 903 CONH₂ 3-pyridyl 1-pyrrolidinocarbonyl 904 CONH₂ 3-pyridyl 2-(methylsulfonyl)phenyl 905 CONH₂ 3-pyridyl 4-morpholino 996 CONH₂ 3-pyridyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 907 CONH₂ 3-pyridyl 4-morpholinocarbonyl 908 CONH₂ 3-pyridyl 2-methyl-1-imidazolyl 909 CONH₂ 3-pyridyl 5-methyl-1-imidazolyl 910 CONH₂ 3-pyridyl 2-methylsulfonyl-1-imidazolyl 911 CONH₂ 2-pyrimidyl 2-(aminosulfonyl)phenyl 912 CONH₂ 2-pyrimidyl 2-(methylaminosulfonyl)phenyl 913 CONH₂ 2-pyrimidyl 1-pyrrolidinocarbonyl 914 CONH₂ 2-pyrimidyl 2-(methylsulfdnyl)phenyl 915 CONH₂ 2-pyrimidyl 4-morpholino 916 CONH₂ 2-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 917 CONH₂ 2-pyrimidyl 4-morpholinocarbonyl 918 CONH₂ 2-pyrimidyl 2-methyl-1-imidazolyl 919 CONH₂ 2-pyrimidyl 5-methyl-1-imidazolyl 920 CONH₂ 2-pyrimidyl 2-methylsulfonyl-1-imidazolyl 921 CONH₂ 5-pyrimidyl 2-(aminosulfonyl)phenyl 922 CONH₂ 5-pyrimidyl 2-(methylaminosulfonyl)phenyl 923 CONH₂ 5-pyrimidyl 1-pyrrolidinocarbonyl 924 CONH₂ 5-pyrimidyl 2-(methylsulfonyl)phenyl 925 CONH₂ 5-pyrimidyl 4-morpholino 926 CONH₂ 5-pyrimidyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 927 CONH₂ 5-pyrimidyl 4-morpholinocarbonyl 928 CONH₂ 5-pyrimidyl 2-methyl-1-imidazolyl 929 CONH₂ 5-pyrimidyl 5-methyl-1-imidazolyl 930 CONH₂ 5-pyrimidyl 2-methylsulfonyl-1-imidazolyl 931 CONH₂ 2-Cl-phenyl 2-(aminosulfonyl)phenyl 932 CONH₂ 2-Cl-phenyl 2-(methylaminosulfonyl)phenyl 933 CONH₂ 2-Cl-phenyl 1-pyrrolidinocarbonyl 934 CONH₂ 2-Cl-phenyl 2-(methylsulfonyl)phenyl 935 CONH₂ 2-Cl-phenyl 4-morpholino 936 CONH₂ 2-Cl-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 937 CONH₂ 2-Cl-phenyl 4-morpholinocarbonyl 938 CONH₂ 2-Cl-phenyl 2-methyl-1-imidazolyl 939 CONH₂ 2-Cl-phenyl 5-methyl-1-imidazolyl 940 CONH₂ 2-Cl-phenyl 2-methylsulfonyl-1-imidazolyl 941 CONH₂ 2-F-phenyl 2-(aminosulfonyl)phenyl 942 CONH₂ 2-F-phenyl 2-(methylaminosulfonyl)phenyl 943 CONH₂ 2-F-phenyl 1-pyrrolidinocarbonyl 944 CONH₂ 2-F-phenyl 2-(methylsulfonyl)phenyl 945 CONH₂ 2-F-phenyl 4-morpholino 946 CONH₂ 2-F-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 947 CONH₂ 2-F-phenyl 4-morpholinocarbonyl 948 CONH₂ 2-F-phenyl 2-methyl-1-imidazolyl 949 CONH₂ 2-F-phenyl 5-methyl-1-imidazolyl 950 CONH₂ 2-F-phenyl 2-methylsulfonyl-1-imidazolyl 951 CONH₂ 2,6-diF-phenyl 2-(aminosulfonyl)phenyl 952 CONH₂ 2,6-diF-phenyl 2-(methylaminosulfonyl)phenyl 953 CONH₂ 2,6-diF-phenyl 1-pyrrolidinocarbonyl 954 CONH₂ 2,6-diF-phenyl 2-(methylsulfonyl)phenyl 955 CONH₂ 2,6-diF-phenyl 4-morpholino 956 CONH₂ 2,6-diF-phenyl 2-(1′-CF₃-tetrazol-2-yl)phenyl 957 CONH₂ 2,6-diF-phenyl 4-morpholinocarbonyl 958 CONH₂ 2,6-diF-phenyl 2-methyl-1-imidazolyl 959 CONH₂ 2,6-diF-phenyl 5-methyl-1-imidazolyl 960 CONH₂ 2,6-diF-phenyl 2-methylsulfonyl-1-imidazolyl

Utility

The compounds of this invention are useful as anticoagulants for the treatment or prevention of thromboembolic disorders in mammals. The term “thromboembolic disorders” as used herein includes arterial or venous cardiovascular or cerebrovascular thromboembolic disorders, including, for example, unstable angina, first or recurrent myocardial infarction, ischemic sudden death, transient ischemic attack, stroke, atherosclerosis, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary and cerebral arterial thrombosis, cerebral embolism, kidney embolisms, and pulmonary embolisms. The anticoagulant effect of compounds of the present invention is believed to be due to inhibition of factor Xa or thrombin.

The effectiveness of compounds of the present invention as inhibitors of factor Xa was determined using purified human factor Xa and synthetic substrate. The rate of factor Xa hydrolysis of chromogenic substrate S2222 (Kabi Pharmacia, Franklin, Ohio) was measured both in the absence and presence of compounds of the present invention. Hydrolysis of the substrate resulted in the release of pNA, which was monitored spectrophotometrically by measuring the increase in absorbance at 405 nM. A decrease in the rate of absorbance change at 405 nm in the presence of inhibitor is indicative of enzyme inhibition. The results of this assay are expressed as inhibitory constant, K_(i).

Factor Xa determinations were made in 0.10 M sodium phosphate buffer, pH 7.5, containing 0.20 M NaCl, and 0.5% PEG 8000. The Michaelis constant, K_(m), for substrate hydrolysis was determined at 25° C. using the method of Lineweaver and Burk. Values of K_(i) were determined by allowing 0.2-0.5 nM human factor Xa (Enzyme Research Laboratories, South Bend, Ind.) to react with the substrate (0.20 mM-1 mM) in the presence of inhibitor. Reactions were allowed to go for 30 minutes and the velocities (rate of absorbance change vs time) were measured in the time frame of 25-30 minutes. The following relationship was used to calculate K_(i) values:

(v _(o) −v _(s))/v _(s)=I/(K_(i)(1+S/K_(m)))

where:

v_(o) is the velocity of the control in the absence of inhibitor;

v_(s) is the velocity in the presence of inhibitor;

I is the concentration of inhibitor;

K_(i) is the dissociation constant of the enzyme:inhibitor complex;

S is the concentration of substrate;

K_(m) is the Michaelis constant.

Using the methodology described above, a number of compounds of the present invention were found to exhibit a K_(i) of ≦10 μM, thereby confirming the utility of the compounds of the present invention as effective Xa inhibitors.

The antithrombotic effect of compounds of the present invention can be demonstrated in a rabbit arterio-venous (AV) shunt thrombosis model. In this model, rabbits weighing 2-3 kg anesthetized with a mixture of xylazine (10 mg/kg i.m.) and ketamine (50 mg/kg i.m.) are used. A saline-filled AV shunt device is connected between the femoral arterial and the femoral venous cannulae. The AV shunt device consists of a piece of 6-cm tygon tubing which contains a piece of silk thread. Blood will flow from the femoral artery via the AV-shunt into the femoral vein. The exposure of flowing blood to a silk thread will induce the formation of a significant thrombus. After forty minutes, the shunt is disconnected and the silk thread covered with thrombus is weighed. Test agents or vehicle will be given (i.v., i.p., s.c., or orally) prior to the opening of the AV shunt. The percentage inhibition of thrombus formation is determined for each treatment group. The ID50 values (dose which produces 50% inhibition of thrombus formation) are estimated by linear regression.

The compounds of formula (I) may also be useful as inhibitors of serine proteases, notably human thrombin, plasma kallikrein and plasmin. Because of their inhibitory action, these compounds are indicated for use in the prevention or treatment of physiological reactions, blood coagulation and inflammation, catalyzed by the aforesaid class of enzymes. Specifically, the compounds have utility as drugs for the treatment of diseases arising from elevated thrombin activity such as myocardial infarction, and as reagents used as anticoagulants in the processing of blood to plasma for diagnostic and other commercial purposes.

Some compounds of the present invention were shown to be direct acting inhibitors of the serine protease thrombin by their ability to inhibit the cleavage of small molecule substrates by thrombin in a purified system. In vitro inhibition constants were determined by the method described by Kettner et al. in J. Biol. Chem. 265, 18289-18297 (1990), herein incorporated by reference. In these assays, thrombin-mediated hydrolysis of the chromogenic substrate S2238 (Helena Laboratories, Beaumont, Tex.) was monitored spectrophotometrically. Addition of an inhibitor to the assay mixture results in decreased absorbance and is indicative of thrombin inhibition. Human thrombin (Enzyme Research Laboratories, Inc., South Bend, Ind.) at a concentration of 0.2 nM in 0.10 M sodium phosphate buffer, pH 7.5, 0.20 M NaCl, and 0.5% PEG 6000, was incubated with various substrate concentrations ranging from 0.20 to 0.02 mM. After 25 to 30 minutes of incubation, thrombin activity was assayed by monitoring the rate of increase in absorbance at 405 nm which arises owing to substrate hydrolysis. Inhibition constants were derived from reciprocal plots of the reaction velocity as a function of substrate concentration using the standard method of Lineweaver and Burk. Using the methodology described above, some compounds of this invention were evaluated and found to exhibit a K_(i) of less than 10 μm, thereby confirming the utility of the compounds of the present invention as effective Xa inhibitors.

The compounds of the present invention can be administered alone or in combination with one or more additional therapeutic agents. These include other anti-coagulant or coagulation inhibitory agents, anti-platelet or platelet inhibitory agents, thrombin inhibitors, or thrombolytic or fibrinolytic agents.

The compounds are administered to a mammal in a therapeutically effective amount. By “therapeutically effective amount” it is meant an amount of a compound of Formula I that, when administered alone or in combination with an additional therapeutic agent to a mammal, is effective to prevent or ameliorate the thromboembolic disease condition or the progression of the disease.

By “administered in combination” or “combination therapy” it is meant that the compound of Formula I and one or more additional therapeutic agents are administered concurrently to the mammal being treated. When administered in combination each component may be administered at the same time or sequentially in any order at different points in time. Thus, each component may be administered separately but sufficiently closely in time so as to provide the desired therapeutic effect. Other anticoagulant agents (or coagulation inhibitory agents) that may be used in combination with the compounds of this invention include warfarin and heparin, as well as other factor Xa inhibitors such as those described in the publications identified above under Background of the Invention.

The term anti-platelet agents (or platelet inhibitory agents), as used herein, denotes agents that inhibit platelet function such as by inhibiting the aggregation, adhesion or granular secretion of platelets. Such agents include, but are not limited to, the various known non-steroidal anti-inflammatory drugs (NSAIDS) such as aspirin, ibuprofen, naproxen, sulindac, indomethacin, mefenamate, droxicam, diclofenac, sulfinpyrazone, and piroxicam, including pharmaceutically acceptable salts or prodrugs thereof. Of the NSAIDS, aspirin (acetylsalicyclic acid or ASA), and piroxicam are preferred. Other suitable anti-platelet agents include ticlopidine, including pharmaceutically acceptable salts or prodrugs thereof. Ticlopidine is also a preferred compound since it is known to be gentle on the gastrointestinal tract in use. Still other suitable platelet inhibitory agents include IIb/IIIa antagonists, thromboxane-A2-receptor antagonists and thromboxane-A2-synthetase inhibitors, as well as pharmaceutically acceptable salts or prodrugs thereof.

The term thrombin inhibitors (or anti-thrombin agents), as used herein, denotes inhibitors of the serine protease thrombin. By inhibiting thrombin, various thrombin-mediated processes, such as thrombin-mediated platelet activation (that is, for example, the aggregation of platelets, and/or the granular secretion of plasminogen activator inhibitor-1 and/or serotonin) and/or fibrin formation are disrupted. A number of thrombin inhibitors are known to one of skill in the art and these inhibitors are contemplated to be used in combination with the present compounds. Such inhibitors include, but are not limited to, boroarginine derivatives, boropeptides, heparins, hirudin and argatroban, including pharmaceutically acceptable salts and prodrugs thereof. Boroarginine derivatives and boropeptides include N-acetyl and peptide derivatives of boronic acid, such as C-terminal a-aminoboronic acid derivatives of lysine, ornithine, arginine, homoarginine and corresponding isothiouronium analogs thereof. The term hirudin, as used herein, includes suitable derivatives or analogs of hirudin, referred to herein as hirulogs, such as disulfatohirudin. Boropeptide thrombin inhibitors include compounds described in Kettner et al., U.S. Pat. No. 5,187,157 and European Patent Application Publication Number 293 881 A2, the disclosures of which are hereby incorporated herein by reference. Other suitable boroarginine derivatives and boropeptide thrombin inhibitors include those disclosed in PCT Application Publication Number 92/07869 and European Patent Application Publication Number 471,651 A2, the disclosures of which are hereby incorporated herein by reference.

The term thrombolytics (or fibrinolytic) agents (or thrombolytics or fibrinolytics), as used herein, denotes agents that lyse blood clots (thrombi). Such agents include tissue plasminogen activator, anistreplase, urokinase or streptokinase, including pharmaceutically acceptable salts or prodrugs thereof. The term anistreplase, as used herein, refers to anisoylated plasminogen streptokinase activator complex, as described, for example, in European Patent Application No. 028,489, the disclosure of which is hereby incorporated herein by reference herein. The term urokinase, as used herein, is intended to denote both dual and single chain urokinase, the latter also being referred to herein as prourokinase.

Administration of the compounds of Formula I of the invention in combination with such additional therapeutic agent, may afford an efficacy advantage over the compounds and agents alone, and may do so while permitting the use of lower doses of each. A lower dosage minimizes the potential of side effects, thereby providing an increased margin of safety.

The compounds of the present invention are also useful as standard or reference compounds, for example as a quality standard or control, in tests or assays involving the inhibition of factor Xa. Such compounds may be provided in a commercial kit, for example, for use in pharmaceutical research involving factor Xa. For example, a compound of the present invention could be used as a reference in an assay to compare its known activity to a compound with an unknown activity. This would ensure the experimenter that the assay was being performed properly and provide a basis for comparison, especially if the test compound was a derivative of the reference compound. When developing new assays or protocols, compounds according to the present invention could be used to test their effectiveness.

The compounds of the present invention may also be used in diagnostic assays involving factor Xa. For example, the presence of factor Xa in an unknown sample could be determined by addition of chromogenic substrate S2222 to a series of solutions containing test sample and optionally one of the compounds of the present invention. If production of pNA is observed in the solutions containing test sample, but no compound of the present invention, then one would conclude factor Xa was present.

Dosage and Formulation

The compounds of this invention can be administered in such oral dosage forms as tablets, capsules (each of which includes sustained release or timed release formulations), pills, powders, granules, elixirs, tinctures, suspensions, syrups, and emulsions. They may also be administered in intravenous (bolus or infusion), intraperitoneal, subcutaneous, or intramuscular form, all using dosage forms well known to those of ordinary skill in the pharmaceutical arts. They can be administered alone, but generally will be administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.

The dosage regimen for the compounds of the present invention will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the species, age, sex, health, medical condition, and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; the route of administration, the renal and hepatic function of the patient,and. the effect desired. A physician or veterinarian can determine and prescribe the effective amount of the drug required to prevent, counter, or arrest the progress of the thromboembolic disorder.

By way of general guidance, the daily oral dosage of each active ingredient, when used for the indicated effects, will range between about 0.001 to 1000 mg/kg of body weight, preferably between about 0.01 to 100 mg/kg of body weight per day, and most preferably between about 1.0 to 20 mg/kg/day. Intravenously, the most preferred doses will range from about 1 to about 10 mg/kg/minute during a constant rate infusion. Compounds of this invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three, or four times daily.

Compounds of this invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using transdermal skin patches. When administered in the form of a transdermal delivery system, the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.

The compounds are typically administered in admixture with suitable pharmaceutical diluents, excipients, or carriers (collectively referred to herein as pharmaceutical carriers) suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixirs, syrups and the like, and consistent with conventional pharmaceutical practices.

For instance, for oral administration in the form of a tablet or capsule, the active drug component can be combined with an oral, non-toxic, pharmaceutically acceptable, inert carrier such as lactose, starch, sucrose, glucose, methyl callulose, magnesium stearate, dicalcium phosphate, calcium sulfate, mannitol, sorbitol and the like; for oral administration in liquid form, the oral drug components can be combined with any oral, non-toxic, pharmaceutically acceptable inert carrier such as ethanol, glycerol, water, and the like. Moreover, when desired or necessary, suitable binders, lubricants, disintegrating agents, and coloring agents can also be incorporated into the mixture. Suitable binders include starch, gelatin, natural sugars such as glucose or beta-lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth, or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes, and the like. Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride, and the like. Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum, and the like.

The compounds of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine, or phosphatidylcholines.

Compounds of the present invention may also be coupled with soluble polymers as targetable drug carriers. Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamide-phenol, polyhydroxyethylaspartamidephenol, or polyethyleneoxidepolylysine substituted with palmitoyl residues. Furthermore, the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and crosslinked or amphipathic block copolymers of hydrogels.

Dosage forms (pharmaceutical compositions) suitable for administration may contain from about 1 milligram to about 100 milligrams of active ingredient per dosage unit. In these pharmaceutical compositions the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.

Gelatin capsules may contain the active ingredient and powdered carriers, such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.

Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.

In general, water, a suitable oil, saline, aqueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances. Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents. Also used are citric acid and its salts and sodium EDTA. In addition, parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol.

Suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences, Mack Publishing Company, a standard reference text in this field.

Representative useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows:

Capsules

A large number of unit capsules can be prepared by filling standard two-piece hard gelatin capsules each with 100 milligrams of powdered active ingredient, 150 milligrams of lactose, 50 milligrams of cellulose, and 6 milligrams magnesium stearate.

Soft Gelatin Capsules

A mixture of active ingredient in a digestable oil such as soybean oil, cottonseed oil or olive oil may be prepared and injected by means of a positive displacement pump into gelatin to form soft gelatin capsules containing 100 milligrams of the active ingredient. The capsules should be washed and dried.

Tablets

Tablets may be prepared by conventional procedures so that the dosage unit is 100 milligrams of active ingredient, 0.2 milligrams of colloidal silicon dioxide, 5 milligrams of magnesium stearate, 275 milligrams of microcrystalline cellulose, 11 milligrams of starch and 98.8 milligrams of lactose. Appropriate coatings may be applied to increase palatability or delay absorption.

Injectable

A parenteral composition suitable for administration by injection may be prepared by stirring 1.5% by weight of active ingredient in 10% by volume propylene glycol and water. The solution should be made isotonic with sodium chloride and sterilized.

Suspension

An aqueous suspension can be prepared for oral administration so that each 5 mL contain 100 mg of finely divided active ingredient, 200 mg of sodium carboxymethyl cellulose, 5 mg of sodium benzoate, 1.0 g of sorbitol solution, U.S.P., and 0.025 mL of vanillin.

Where the compounds of this invention are combined with other anticoagulant agents, for example, a daily dosage may be about 0.1 to 100 milligrams of the compound of Formula I and about 1 to 7.5 milligrams of the second anticoagulant, per kilogram of patient body weight. For a tablet dosage form, the compounds of this invention generally may be present in an amount of about 5 to 10 milligrams per dosage unit, and the second anti-coagulant in an amount of about 1 to 5 milligrams per dosage unit.

Where the compounds of Formula I are administered in combination with an anti-platelet agent, by way of general guidance, typically a daily dosage may be about 0.01 to 25 milligrams of the compound of Formula I and about 50 to 150 milligrams of the anti-platelet agent, preferably about 0.1 to 1 milligrams of the compound of Formula I and about 1 to 3 milligrams of antiplatelet agents, per kilogram of patient body weight.

Where the compounds of Formula I are adminstered in combination with thrombolytic agent, typically a daily dosage may be about 0.1 to 1 milligrams of the compound of Formula I, per kilogram of patient body weight and, in the case of the thrombolytic agents, the usual dosage of the thrombolyic agent when administered alone may be reduced by about 70-80% when administered with a compound of Formula I.

Where two or more of the foregoing second therapeutic agents are administered with the compound of Formula I, generally the amount of each component in a typical daily dosage and typical dosage form may be reduced relative to the usual dosage of the agent when administered alone, in view of the additive or synergistic effect of the therapeutic agents when administered in combination.

Particularly when provided as a single dosage unit, the potential exists for a chemical interaction between the combined active ingredients. For this reason, when the compound of Formula I and a second therapeutic agent are combined in a single dosage unit they are formulated such that although the active ingredients are combined in a single dosage unit, the physical contact between the active ingredients is minimized (that is, reduced). For example, one active ingredient may be enteric coated. By enteric coating one of the active ingredients, it is possible not only to minimize the contact between the combined active ingredients, but also, it is possible to control the release of one of these components in the gastrointestinal tract such that one of these components is not released in the stomach but rather is released in the intestines. One of the active ingredients may also be coated with a material which effects a sustained-release throughout the gastrointestinal tract and also serves to minimize physical contact between the combined active ingredients. Furthermore, the sustained-released component can be additionally enteric coated such that the release of this component occurs only in the intestine. Still another approach would involve the formulation of a combination product in which the one component is coated with a sustained and/or enteric release polymer, and the other component is also coated with a polymer such as a lowviscosity grade of hydroxypropyl methylcellulose (HPMC) or other appropriate materials as known in the art, in order to further separate the active components. The polymer coating serves to form an additional barrier to interaction with the other component.

These as well as other ways of minimizing contact between the components of combination products of the present invention, whether administered in a single dosage form or administered in separate forms but at the same time by the same manner, will be readily apparent to those skilled in the art, once armed with the present disclosure.

Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise that as specifically described herein. 

What is claimed as new and desired to be secured by Letter Patent of United States is:
 1. A compound of formula Ib:

or a stereoisomer or pharmaceutically acceptable salt thereof, wherein; J is O D is selected from C(═NR⁸)NR⁷R⁹, and CR⁸R⁹NR⁷R⁸, provided that D is substituted meta on E; E is phenyl substituted with 1 R; R is selected from H, halogen, OR³, (CH₂)OR³, C₁₋₄ alkyl, OCF₃, and CF₃; Z is C(O)NH, provided that Z does not form a N—N bond with group A; R^(1a) is absent or selected from —(CH₂)_(r)-R¹′, NCH₂R¹″, OCH₂R¹″, SCH₂R¹″, N(CH₂)₂(CH₂)_(t)R¹′, O(CH₂)₂(CH₂)_(t)R¹′, and S(CH₂)₂(CH₂)_(t)R¹′; R¹′ is selected from H, C₁₋₃ alkyl, halo, (CF₂)_(r)CF₃, OR², NR²R^(2a), C(O)R^(2c), OC(O)R², (CF₂)_(r)CO₂R^(2c), S(O)_(p)R^(2b), NR²(CH₂)_(r)OR², NR²C(O)R^(2b), NR²C(O)NHR^(2b), NR²C(O)₂R^(2a), OC(O)NR^(2b), C(O)NR²R^(2a), SO₂NR²R^(2a), NR²SO₂R^(2b), and C₃₋₆ carbocyclic residue substituted with 0-2 R⁴; R¹″ is selected from H, C(O)R^(2b), C(O)NR²R^(2a), S(O)R^(2b), S(O)₂R^(2b), and SO₂NR²R^(2a); R², at each occurrence, is selected from H, CF₃, C₁₋₆ alkyl, benzyl, and C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b); R^(2a), at each occurrence, is selected from H, CF₃, C₁₋₆ alkyl, benzyl, and C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b); R^(2b), at each occurrence, is selected from CF₃, C₁₋₄ alkoxy, C₁₋₆ alkyl, benzyl, and C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b); R^(2c), at each occurrence, is selected from CF₃, OH, C₁₋₄ alkoxy, C₁₋₆ alkyl, benzyl, and C₃₋₆ carbocyclic residue substituted with 0-2 R^(4b); R³, at each occurrence, is selected from H, C₁₋₄ alkyl, and phenyl; R^(3a), at each occurrence, is selected from H, C₁₋₄ alkyl, and phenyl; A is selected from: C₃₋₁₀ carbocyclic residue substituted with 0-2 R⁴, and pyridyl substituted with 0-2 R⁴; B is selected from: Y, X—Y, NR²R^(2a), C(═NR²)NR²R^(2a), NR²C(═NR²)NR²R^(2a), C₃₋₁₀ carbocyclic residue substituted with 0-2 R^(4a), and pyridyl substituted with 0-2 R^(4a); X is selected from C₁₋₄ alkylene, —CR²(CR²R^(2b))(CH₂)_(t)—, —C(O)—, —C(═NR)—, —CR²(NR¹″R²)—, —CR²(OR²)—, —CR²(SR²)—, —C(O)CR²R^(2a)—, —CR²R^(2a)C(O), —S(O)_(p)—, —S(O)_(p)CR²R^(2a)—, —CR²R^(2a)S(O)_(p)—, —S(O)₂NR²—, —NR²S(O)₂—, —NR²S(O)₂CR²R^(2a)—, —CR²R^(2a)S(O)₂NR²—, —NR²S(O)₂NR²—, —C(O)NR²—, —NR²C(O)—, —C(O)NR²CR²R^(2a)—, —NR²C(O)CR²R^(2a)—, —CR²R^(2a)C(O)NR²—, —CR²R^(2a)NR²C(O)—, —NR²C(O)O—, —OC(O)NR²—, —NR²C(O)NR²—, —NR²—, —NR²CR²R^(2a)—, —CR²R^(2a)NR²—, O, —CR²R^(2a)O—, and —OCR²R^(2a)—; Y is selected from: (CH₂)_(r)NR²R^(2a), provided that X—Y do not form a N—N, O—N, or S—N bond and that X is other than a group terminating with C(O), C₃₋₁₀ carbocyclic residue substituted with 0-2 R^(4a), and pyridyl substituted with 0-2 R^(4a); R⁴, at each occurrence, is selected from ═O, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, —CN, NO₂, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), NR²C(O)NR²R^(2a), C(═NR²)NR²R^(2a), NHC(═NR²)NR²R^(2a), SO₂NR²R^(2a), NR²SO₂NR²R^(2a), NR²SO₂—C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, (CF₂)_(r)CF₃, NCH₂R¹″, OCH₂R¹″, SCH₂R¹″, N(CH₂)₂(CH₂)_(t)R¹′, O(CH₂)₂(CH₂)_(t)R¹′, and S(CH₂)₂(CH₂)_(t)R¹′; alternatively, one R⁴ is pyridyl; R^(4a), at each occurrence, is selected from ═O, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, —CN, NO₂, (CH₂)_(r)NR²R^(2a), NR²C(O)R^(2b), C(O)NR²R^(2a), NR²C(O)NR²R^(2a), C(═NR²)NR²R^(2a), NHC(═NR²)NR²R^(2a), SO₂NR²R^(2a), NR²SO₂NR²R^(2a), NR²SO₂—C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, and (CF₂)_(r)CF₃; alternatively, one R^(4a) is pyridyl; R^(4b), at each occurrence, is selected from ═O, (CH₂)_(r)OR³, halo, C₁₋₄ alkyl, —CN, NO₂, (CH₂)_(r)NR³R^(3a), (CH₂)_(r)C(O)R³, NR³O(O)R^(3a), C(O)NR³R^(3a), NR³C(O)NR³R^(3a), C(═NR³)NR³R^(3a), NH³C(═NR³)NR³R^(3a), SO₂NR³R^(3a), NR³SO₂NR³R^(3a), NR³SO₂-C₁₋₄ alkyl, NR³SO₂CF₃, NR³SO₂-phenyl, S(O)_(p)CF₃, S(O)_(p)-C₁₋₄ alkyl, S(O)_(p)-phenyl, and (CF₂)_(r)CF₃; R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl substituted with 0-2 R⁶, and benzyl substituted with 0-2 R⁶; R⁶, at each occurrence, is selected from H, OH, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, CN, NO₂, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), NR²C(O)NR²R^(2a), C(═NH)NH₂, NHC(═NR)NH₂, SO₂NR²R^(2a), NR²SO₂NR²R^(2a), and NR²SO₂C₁₋₄ alkyl; R⁷, at each occurrence, is selected from H, OH, C₁₋₆ alkyl, C₁₋₆ alkylcarbonyl, C₁₋₆ alkoxy, C₁₋₄ alkoxycarbonyl, (CH₂)_(n)-phenyl, C₆₋₁₀ aryloxy, C₆₋₁₀ aryloxycarbonyl, C₆₋₁₀ arylmethylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₆₋₁₀ arylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₁₋₆ alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C₁₋₄ alkoxycarbonyl; R⁸, at each occurrence, is selected from H, C₁₋₆ alkyl and (CH₂)_(n)-phenyl; R⁹, at each occurrence, is selected from H, C₁₋₆ alkyl and (CH₂)_(n)-phenyl; n, at each occurrence, is selected from 0, 1, 2, and 3; p, at each occurrence, is selected from 0, 1, and 2; r, at each occurrence, is selected from 0, 1, 2, and 3; and, t, at each occurrence, is selected from 0 and 1; provided that D—E— and —Z—A—B are not both benzamidines and B is other than C(O)(CH₂)_(r)NR²R^(2a).
 2. A compound according to claim 1, wherein the compound is of formula Ib:

wherein, groups D—E— and —Z—A—B are attached to adjacent atoms on the ring; A is phenyl or pyridyl substituted with 0-2 R⁴; B is selected from: Y, X—Y, NR²R^(2a), C(═NR²)NR²R^(2a), and NR²C(═NR²)NR²R^(2a); X is selected from C₁₋₄ alkylene, —C(O)—, —C(═NR)—, —CR²(NR²R^(2a))—, —C(O)CR²R^(2a)—, —CR²R^(2a)C(O), —C(O)NR²—, —NR²C(O)—, —C(O)NR²CR²R^(2a)—, —NR²C(O)CR²R^(2a)—, —CR²R^(2a)C(O)NR²—, —CR²R^(2a)NR²C(O)—, —NR²C(O)NR²—, —NR²—, —NR²CR²R^(2a)—, —CR²R^(2a)NR²—, O, —CR²R^(2a)O—, and —OCR²R^(2a)—; Y is NR²R^(2a), provided that X—Y do not form a N—N or O—N bond and that X is other than a group terminating with C(O); alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a); cyclopropyl, cyclopentyl, cyclohexyl, phenyl, and pyridyl.
 3. A compound according to claim 2, wherein the compound is of formula Ib and is selected from:

wherein; J is O.
 4. A compound according to claim 3, wherein the compound is of formula Ib: D is selected from C(═NH)NH₂, CH₂NH₂, CH₂NHCH₃, CH(CH₃)NH₂, and C(CH₃)₂NH₂, provided that D is substituted meta to ring M on E; and, R is selected from H, OCH₃, Cl, and E.
 5. A compound according to claim 4, wherein the compound is of formula Ib: D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, and 4-fluoro-3-(methylaminomethyl)phenyl.
 6. A compound according to claim 3, wherein the compound is of formula Ib: A is selected from phenyl and pyridyl and is substituted with 0-2 R⁴; and, B is phenyl and is substituted with 0-1 R^(4a); R⁴, at each occurrence, is selected from OH, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), and (CF₂)_(r)CF₃; R^(4a) is selected from C₁₋₄ alkyl, CF₃, S(O)_(p)R⁵, and SO₂NR²R^(2a); R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl, and benzyl.
 7. A compound according to claim 6, wherein the compound is of formula Ib: A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and, B is selected from the group: 2-CF₃-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, and 2-(methylsulfonyl)phenyl.
 8. A compound according to claim 3, wherein the compound is of formula Ib: D is selected from C(═NH)NH₂, CH₂NH₂, CH₂NHCH₃, CH(CH₃)NH₂, and C(CH₃)₂NH₂, provided that D is substituted meta to ring M on E; R is selected from H, OCH₃, Cl, and F; A is selected from phenyl and pyridyl and is substituted with 0-2 R⁴; and, B is phenyl and is substituted with 0-1 R^(4a); R⁴, at each occurrence, is selected from OH, (CH₂)_(r)OR², halo, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), and (CF₂)_(r)CF₃; R^(4a) is selected from C₁₋₄ alkyl, CF₃, S(O)_(p)R⁵, and SO₂NR²R^(2a); R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl, and benzyl.
 9. A compound according to claim 8, wherein the compound is of formula Ib: D—E is selected from 3-amidinophenyl, 3-aminomethylphenyl, 3-(methylaminomethyl)phenyl, 3-(1-aminoethyl)phenyl, 3-(2-amino-2-propyl)phenyl, 4-chloro-3-amidinophenyl, 4-chloro-3-aminomethylphenyl, 4-chloro-3-(methylaminomethyl)phenyl, 4-fluoro-3-amidinophenyl, 4-fluoro-3-aminomethylphenyl, and 4-fluoro-3-(methylaminomethyl)phenyl; A is selected from the group: phenyl, 2-pyridyl, 3-pyridyl, 2-Cl-phenyl, 3-Cl-phenyl, 2-F-phenyl, 3-F-phenyl, 2-methylphenyl, 2-aminophenyl, and 2-methoxyphenyl; and, B is selected from the group: 2-CF₃-phenyl, 2-(aminosulfonyl)phenyl, 2-(methylaminosulfonyl)phenyl, 2-(dimethylaminosulfonyl)phenyl, and 2-(methylsulfonyl)phenyl.
 10. A compound according to claim 9, wherein the compound is of formula Ib₁.
 11. A compound according to claim 9, wherein the compound is of formula Ib₂.
 12. A compound according to claim 9, wherein the compound is of formula Ib₃.
 13. A compound according to claim 9, wherein the compound is of formula Ib₄.
 14. A compound according to claim 3, wherein the compound is of formula Ib₂: D is selected from C(═NR⁸)NR⁷R⁹ and CH₂NR⁷R⁸, provided that D is substituted meta to ring M on E; R is selected from H, Cl, F, OR³, CH₃, CH₂CH₃, OCF₃, and CF₃; R^(1a) is absent or selected from —(CH₂)_(r)-R¹′, NCH₂R¹″, OCH₂R¹″, SCH₂R¹″, N(CH₂)₂(CH₂)_(t)R¹′, O(CH₂)₂(CH₂)_(t)R¹′, and S(CH₂)₂(CH₂)_(t)R¹′; R¹′, at each occurrence, is selected from H, C₁₋₃ alkyl, halo, (CF₂)_(r)CF₃, OR², NR²R^(2a), C(O)R^(2c), (CF₂)_(r)CO₂R^(2c), S(O)_(p)R^(2b), NR²(CH₂)_(r)OR², NR²C(O)R^(2b), NR²C(O)₂R^(2b), C(O)NR²R^(2a), SO₂NR²R^(2a), and NR²SO₂R^(2b); A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R⁴; phenyl and pyridyl; B is selected from: Y, X—Y, NR²R^(2a), C(═NR²)NR²R^(2a), and NR²C(═NR²)NR²R^(2a); X is selected from CH₂, —CR²(CR²R^(2b))(CH₂)_(t)—, —C(O)—, —C(═NR)—, —CH(NR²R^(2a))—, —C(O)NR²—, —NR²C(O)—, —NR²C(O)NR²—, —NR²—, and O; Y is NR²R^(2a), provided that X—Y do not form a N—N or O—N bond and that X is other than a group terminating with C(O); alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a); phenyl and pyridyl; R⁴, at each occurrence, is selected from ═O, OH, Cl, F, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), C(═NH)NH₂, NHC(═NH)NH₂, SO₂NR²R^(2a), NR²SO₂-C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, and (CF₂)_(r)CF₃; R^(4a), at each occurrence, is selected from ═O, OH, Cl, F, C₁₋₄ alkyl, (CH₂)_(r)NR²R^(2a), NR²C(O)R^(2b), C(O)NR²R^(2a), C(═NH)NH₂, NHC(═NH)NH₂, SO₂NR²R^(2a), NR²SO₂-C₁₋₄ alkyl, NR²SO₂R⁵, S(O)_(p)R⁵, and (CF₂)_(r)CF₃; R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl substituted with 0-2 R⁶, and benzyl substituted with 0-2 R⁶; R⁶, at each occurrence, is selected from H, ═O, OH, OR², Cl, F, CH₃, CN, NO₂, (CH₂)_(r)NR²R^(2a), (CH₂)_(r)C(O)R^(2b), NR²C(O)R^(2b), C(═NH)NH₂, NHC(═NH)NH₂, and SO₂NR²R^(2a); R⁷, at each occurrence, is selected from H, OH, C₁₋₆ alkyl, C₁₋₆ alkylcarbonyl, C₁₋₆ alkoxy, C₁₋₄ alkoxycarbonyl, benzyl, C₆₋₁₀ aryloxy, C₆₋₁₀ aryloxycarbonyl, C₆₋₁₀ arylmethylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₆₋₁₀ arylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₁₋₆ alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C₁₋₄ alkoxycarbonyl; R⁸, at each occurrence, is selected from H, C₁₋₆ alkyl and benzyl; and R⁹, at each occurrence, is selected from H, C₁₋₆ alkyl and benzyl.
 15. A compound according to claim 14, wherein the compound is of formula Ib: R is selected from H, Cl, F, OCH₃, CH₃, OCF₃, and CF₃; R^(1a) is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2c), CH₂C(O)R^(2c), C(O)NR²R^(2a), and SO₂NR²R^(2a); R^(1b) is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2c), CH₂C(O)R^(2c), C(O)NR²R^(2a), and SO₂NR²R^(2a); A is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R⁴; phenyl and pyridyl; B is selected from: Y and X—Y; X is selected from CH₂, —CR²(CR²R^(2b))—, —C(O)—, —C(═NR)—, —CH(NR²R^(2a))—, —C(O)NR²—, —NR²C(O)—, —NR²C(O)NR²—, —NR²—, and O; Y is NR²R^(2a), provided that X—Y do not form a N—N or O—N bond and that X is other than a group terminating with C(O); alternatively, Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a); phenyl and pyridyl; R², at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl; R^(2a), at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl; R^(2b), at each occurrence, is selected from CF₃, OCH₃, CH₃, benzyl, and phenyl; R^(2c), at each occurrence, is selected from CF₃, OH, OCH₃, CH₃, benzyl, and phenyl; R³, at each occurrence, is selected from H, CH₃, CH₂CH₃, and phenyl; R^(3a), at each occurrence, is selected from H, CH₃, CH₂CH₃, and phenyl; R⁴, at each occurrence, is selected from OH, Cl, F, CH₃, CH₂CH₃, NR²R^(2a), CH₂NR²R^(2a), C(O)R^(2b), NR²C(O)R^(2b), C(O)NR²R^(2a), and CF₃; R^(4a), at each occurrence, is selected from OH, Cl, F, CH₃, CH₂CH₃, NR²R^(2a), CH₂NR²R^(2a), C(O)NR²R^(2a), SO₂NR²R^(2a), S(O)_(p)R⁵, and CF₃; R⁵, at each occurrence, is selected from CF₃, C₁₋₆ alkyl, phenyl substituted with 0-2 R⁶, and benzyl substituted with 1 R⁶; R⁶, at each occurrence, is selected from H, OH, OCH₃, Cl, F, CH₃, CN, NO₂, NR²R^(2a), CH₂NR²R^(2a), and SO₂NR²R^(2a); R⁷, at each occurrence, is selected from H, OH, C₁₋₃ alkyl, C₁₋₃ alkylcarbonyl, C₁₋₃ alkoxy, C₁₋₄ alkoxycarbonyl, benzyl, phenoxy, phenoxycarbonyl, benzylcarbonyl, C₁₋₄ alkylcarbonyloxy C₁₋₄ alkoxycarbonyl, phenylcarbonyloxy C₁₋₄ alkoxycarbonyl, C₁₋₆ alkylaminocarbonyl, phenylaminocarbonyl, and phenyl C₁₋₄ alkoxycarbonyl; R⁸, at each occurrence, is selected from H, CH₃, and benzyl; and, R⁹, at each occurrence, is selected from H, CH₃, and benzyl.
 16. A compound according to claim 15, wherein the compound is of formula Ib₂: R^(1a) is absent or is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), C(O)NR²R^(2a), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2c), CH₂C(O)R^(2c), and SO₂NR²R^(2a); R^(1b) is absent or is selected from H, CH₃, CH₂CH₃, Cl, F, CF₃, OCH₃, NR²R^(2a), S(O)_(p)R^(2b), C(O)NR²R^(2a), CH₂S(O)_(p)R^(2b), CH₂NR²S(O)_(p)R^(2b), C(O)R^(2b), CH₂C(O)R^(2b), and SO₂NR²R^(2a); B is selected from: Y and X—Y; X is selected from —C(O)— and O; Y is selected from one of the following carbocyclic and heterocyclic systems which are substituted with 0-2 R^(4a); phenyl, and pyridyl, R², at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl; R^(2a), at each occurrence, is selected from H, CF₃, CH₃, benzyl, and phenyl; R^(2b), at each occurrence, is selected from CF₃, OCH₃, CH₃, benzyl, and phenyl; R^(2c), at each occurrence, is selected froim CF₃, OH, OCH₃, CH₃, benzyl, and phenyl; R⁴, at each occurrence, is selected from Cl, F, CH₃, NR²R^(2a), and CF₃; R^(4a), at each occurrence, is selected from Cl, F, CH₃, SO₂NR²R^(2a), S(O)_(p)R⁵, and CF₄; and, R⁵, at each occurrence, is selected from CF₃ and CH₃.
 17. A compound according to claim 1, wherein the compound is selected from the group: 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarboryyl]-5-(hydroxymethyl)isoxazole; 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; 3-(3-amidinophenyl)-4-[(2′-methylsulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; 3-(3-amidinophenyl)-4-[5-(2-aminosulfonyl)phenylpyrid-2-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole; 3-(3-amidinophenyl)-4-[(2′-trifluoromethyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(trifluoromethyl)isoxazole; 3-(3-amidinophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)-isoxazole; 3-(3-amidinophenyl)-4-[(2′-t-butylaminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; 3-(3-amidinophenyl)-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]-5-(methoxymethyl)isoxazole; 3-(3-amidinophenyl)-4-[(3-fluoro-2′-methylsulfonyl-[1,1′]-biphe-4-yl)aminocarbonyl]isoxazole; 3-(3-amidinophenyl)-4-[(2′-trifluoromethylthio-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; and, 3-(3-amidinophenyl)-5-amino-4-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)aminocarbonyl]isoxazole; or a pharmaceutically acceptable salt thereof.
 18. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 1 or a pharmaceutically acceptable salt thereof.
 19. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 2 or a pharmaceutically acceptable salt thereof.
 20. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 3 or a pharmaceutically acceptable salt thereof.
 21. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 14 or a pharmaceutically acceptable salt thereof.
 22. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 17 or a pharmaceutically acceptable salt thereof.
 23. A method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound according to claim 1 or a pharmaceutically acceptable salt thereof.
 24. A method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound according to claim 2 or a pharmaceutically acceptable salt thereof.
 25. A method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound according to claim 3 or a pharmaceutically acceptable salt thereof.
 26. A method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound according to claim 14 or a pharmaceutically acceptable salt thereof.
 27. A method for treating or preventing a thromboembolic disorder, comprising: administering to a patient in need thereof a therapeutically effective amount of a compound according to claim 17 or a pharmaceutically acceptable salt thereof. 